Name: rs10037007
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs10037007

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:170981958 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: A>C / A>G / A>T
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.333010 (100467/301694, ALFA)
A=0.468616 (124038/264690, TOPMED)
A=0.328776 (67424/205076, GENOGRAPHIC) (+ 22 more)
A=0.463372 (64848/139948, GnomAD)
G=0.45471 (35652/78406, PAGE_STUDY)
A=0.24598 (6951/28258, 14KJPN)
A=0.24523 (4110/16760, 8.3KJPN)
A=0.4528 (2900/6404, 1000G_30x)
A=0.4417 (2212/5008, 1000G)
A=0.3371 (1510/4480, Estonian)
A=0.3127 (1205/3854, ALSPAC)
A=0.3188 (1182/3708, TWINSUK)
A=0.2846 (834/2930, KOREAN)
A=0.3671 (765/2084, HGDP_Stanford)
A=0.4804 (907/1888, HapMap)
A=0.2636 (483/1832, Korea1K)
A=0.303 (302/998, GoNL)
A=0.308 (243/788, PRJEB37584)
A=0.310 (186/600, NorthernSweden)
A=0.233 (95/408, SGDP_PRJ)
A=0.333 (72/216, Qatari)
A=0.338 (73/216, Vietnamese)
A=0.45 (26/58, Ancient Sardinia)
A=0.20 (10/50, Siberian)
A=0.40 (16/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RANBP17 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	301694	A=0.333010	G=0.666990
European	Sub	267426	A=0.320818	G=0.679182
African	Sub	7952	A=0.7569	G=0.2431
African Others	Sub	318	A=0.855	G=0.145
African American	Sub	7634	A=0.7528	G=0.2472
Asian	Sub	3936	A=0.3219	G=0.6781
East Asian	Sub	3192	A=0.2851	G=0.7149
Other Asian	Sub	744	A=0.480	G=0.520
Latin American 1	Sub	1134	A=0.4118	G=0.5882
Latin American 2	Sub	7216	A=0.3915	G=0.6085
South Asian	Sub	5224	A=0.1863	G=0.8137
Other	Sub	8806	A=0.3544	G=0.6456

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	301694	A=0.333010	G=0.666990
Allele Frequency Aggregator	European	Sub	267426	A=0.320818	G=0.679182
Allele Frequency Aggregator	Other	Sub	8806	A=0.3544	G=0.6456
Allele Frequency Aggregator	African	Sub	7952	A=0.7569	G=0.2431
Allele Frequency Aggregator	Latin American 2	Sub	7216	A=0.3915	G=0.6085
Allele Frequency Aggregator	South Asian	Sub	5224	A=0.1863	G=0.8137
Allele Frequency Aggregator	Asian	Sub	3936	A=0.3219	G=0.6781
Allele Frequency Aggregator	Latin American 1	Sub	1134	A=0.4118	G=0.5882
TopMed	Global	Study-wide	264690	A=0.468616	G=0.531384
Genographic Project	Global	Study-wide	205076	A=0.328776	G=0.671224
gnomAD - Genomes	Global	Study-wide	139948	A=0.463372	G=0.536628
gnomAD - Genomes	European	Sub	75826	A=0.32400	G=0.67600
gnomAD - Genomes	African	Sub	41910	A=0.76161	G=0.23839
gnomAD - Genomes	American	Sub	13618	A=0.39683	G=0.60317
gnomAD - Genomes	Ashkenazi Jewish	Sub	3318	A=0.3267	G=0.6733
gnomAD - Genomes	East Asian	Sub	3128	A=0.3082	G=0.6918
gnomAD - Genomes	Other	Sub	2148	A=0.4232	G=0.5768
The PAGE Study	Global	Study-wide	78406	A=0.54529	G=0.45471
The PAGE Study	AfricanAmerican	Sub	32386	A=0.75011	G=0.24989
The PAGE Study	Mexican	Sub	10768	A=0.37342	G=0.62658
The PAGE Study	Asian	Sub	8296	A=0.2629	G=0.7371
The PAGE Study	PuertoRican	Sub	7886	A=0.4688	G=0.5312
The PAGE Study	NativeHawaiian	Sub	4518	A=0.4608	G=0.5392
The PAGE Study	Cuban	Sub	4216	A=0.4156	G=0.5844
The PAGE Study	Dominican	Sub	3804	A=0.5555	G=0.4445
The PAGE Study	CentralAmerican	Sub	2444	A=0.4521	G=0.5479
The PAGE Study	SouthAmerican	Sub	1976	A=0.4145	G=0.5855
The PAGE Study	NativeAmerican	Sub	1258	A=0.4030	G=0.5970
The PAGE Study	SouthAsian	Sub	854	A=0.215	G=0.785
14KJPN	JAPANESE	Study-wide	28258	A=0.24598	G=0.75402
8.3KJPN	JAPANESE	Study-wide	16760	A=0.24523	G=0.75477
1000Genomes_30x	Global	Study-wide	6404	A=0.4528	G=0.5472
1000Genomes_30x	African	Sub	1786	A=0.8343	G=0.1657
1000Genomes_30x	Europe	Sub	1266	A=0.3207	G=0.6793
1000Genomes_30x	South Asian	Sub	1202	A=0.1897	G=0.8103
1000Genomes_30x	East Asian	Sub	1170	A=0.3111	G=0.6889
1000Genomes_30x	American	Sub	980	A=0.420	G=0.580
1000Genomes	Global	Study-wide	5008	A=0.4417	G=0.5583
1000Genomes	African	Sub	1322	A=0.8336	G=0.1664
1000Genomes	East Asian	Sub	1008	A=0.3046	G=0.6954
1000Genomes	Europe	Sub	1006	A=0.3171	G=0.6829
1000Genomes	South Asian	Sub	978	A=0.189	G=0.811
1000Genomes	American	Sub	694	A=0.431	G=0.569
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.3371	G=0.6629
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.3127	G=0.6873
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.3188	G=0.6812
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.2846	C=0.0000, G=0.7154, T=0.0000
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	A=0.3671	G=0.6329
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	A=0.296	G=0.704
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	A=0.215	G=0.785
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	A=0.257	G=0.743
HGDP-CEPH-db Supplement 1	Europe	Sub	320	A=0.322	G=0.678
HGDP-CEPH-db Supplement 1	Africa	Sub	242	A=0.872	G=0.128
HGDP-CEPH-db Supplement 1	America	Sub	216	A=0.324	G=0.676
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	A=0.88	G=0.12
HapMap	Global	Study-wide	1888	A=0.4804	G=0.5196
HapMap	American	Sub	770	A=0.329	G=0.671
HapMap	African	Sub	688	A=0.776	G=0.224
HapMap	Asian	Sub	254	A=0.272	G=0.728
HapMap	Europe	Sub	176	A=0.290	G=0.710
Korean Genome Project	KOREAN	Study-wide	1832	A=0.2636	G=0.7364
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.303	G=0.697
CNV burdens in cranial meningiomas	Global	Study-wide	788	A=0.308	G=0.692
CNV burdens in cranial meningiomas	CRM	Sub	788	A=0.308	G=0.692
Northern Sweden	ACPOP	Study-wide	600	A=0.310	G=0.690
SGDP_PRJ	Global	Study-wide	408	A=0.233	G=0.767
Qatari	Global	Study-wide	216	A=0.333	G=0.667
A Vietnamese Genetic Variation Database	Global	Study-wide	216	A=0.338	G=0.662
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	58	A=0.45	G=0.55
Siberian	Global	Study-wide	50	A=0.20	G=0.80
The Danish reference pan genome	Danish	Study-wide	40	A=0.40	G=0.60

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 5	NC_000005.10:g.170981958A>C
GRCh38.p14 chr 5	NC_000005.10:g.170981958A>G
GRCh38.p14 chr 5	NC_000005.10:g.170981958A>T
GRCh37.p13 chr 5	NC_000005.9:g.170408962A>C
GRCh37.p13 chr 5	NC_000005.9:g.170408962A>G
GRCh37.p13 chr 5	NC_000005.9:g.170408962A>T

Gene: RANBP17, RAN binding protein 17 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RANBP17 transcript	NM_022897.5:c.1710+13581A… NM_022897.5:c.1710+13581A>C	N/A	Intron Variant
RANBP17 transcript variant X1	XM_011534627.2:c.1710+135… XM_011534627.2:c.1710+13581A>C	N/A	Intron Variant
RANBP17 transcript variant X14	XM_011534636.3:c.1710+135… XM_011534636.3:c.1710+13581A>C	N/A	Intron Variant
RANBP17 transcript variant X19	XM_011534637.3:c.1710+135… XM_011534637.3:c.1710+13581A>C	N/A	Intron Variant
RANBP17 transcript variant X2	XM_017009736.2:c.1590+135… XM_017009736.2:c.1590+13581A>C	N/A	Intron Variant
RANBP17 transcript variant X4	XM_017009738.2:c.1563+135… XM_017009738.2:c.1563+13581A>C	N/A	Intron Variant
RANBP17 transcript variant X5	XM_017009739.2:c.1563+135… XM_017009739.2:c.1563+13581A>C	N/A	Intron Variant
RANBP17 transcript variant X6	XM_017009740.2:c.1443+135… XM_017009740.2:c.1443+13581A>C	N/A	Intron Variant
RANBP17 transcript variant X7	XM_017009741.3:c.1710+135… XM_017009741.3:c.1710+13581A>C	N/A	Intron Variant
RANBP17 transcript variant X8	XM_017009742.3:c.1710+135… XM_017009742.3:c.1710+13581A>C	N/A	Intron Variant
RANBP17 transcript variant X10	XM_017009744.2:c.1710+135… XM_017009744.2:c.1710+13581A>C	N/A	Intron Variant
RANBP17 transcript variant X12	XM_017009745.2:c.810+1358… XM_017009745.2:c.810+13581A>C	N/A	Intron Variant
RANBP17 transcript variant X15	XM_017009746.3:c.1711-110… XM_017009746.3:c.1711-1107A>C	N/A	Intron Variant
RANBP17 transcript variant X3	XM_047417530.1:c.1590+135… XM_047417530.1:c.1590+13581A>C	N/A	Intron Variant
RANBP17 transcript variant X11	XM_047417531.1:c.1710+135… XM_047417531.1:c.1710+13581A>C	N/A	Intron Variant
RANBP17 transcript variant X13	XM_047417532.1:c.1590+135… XM_047417532.1:c.1590+13581A>C	N/A	Intron Variant
RANBP17 transcript variant X20	XM_047417533.1:c.159+1358… XM_047417533.1:c.159+13581A>C	N/A	Intron Variant
RANBP17 transcript variant X21	XM_017009747.2:c.	N/A	Genic Upstream Transcript Variant
RANBP17 transcript variant X9	XR_007058628.1:n.	N/A	Intron Variant
RANBP17 transcript variant X16	XR_007058629.1:n.	N/A	Intron Variant
RANBP17 transcript variant X18	XR_007058630.1:n.	N/A	Intron Variant
RANBP17 transcript variant X17	XR_941108.3:n.	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	A=	C	G	T
GRCh38.p14 chr 5	NC_000005.10:g.170981958=	NC_000005.10:g.170981958A>C	NC_000005.10:g.170981958A>G	NC_000005.10:g.170981958A>T
GRCh37.p13 chr 5	NC_000005.9:g.170408962=	NC_000005.9:g.170408962A>C	NC_000005.9:g.170408962A>G	NC_000005.9:g.170408962A>T
RANBP17 transcript	NM_022897.3:c.1710+13581=	NM_022897.3:c.1710+13581A>C	NM_022897.3:c.1710+13581A>G	NM_022897.3:c.1710+13581A>T
RANBP17 transcript	NM_022897.5:c.1710+13581=	NM_022897.5:c.1710+13581A>C	NM_022897.5:c.1710+13581A>G	NM_022897.5:c.1710+13581A>T
RANBP17 transcript variant X1	XM_011534627.2:c.1710+13581=	XM_011534627.2:c.1710+13581A>C	XM_011534627.2:c.1710+13581A>G	XM_011534627.2:c.1710+13581A>T
RANBP17 transcript variant X14	XM_011534636.3:c.1710+13581=	XM_011534636.3:c.1710+13581A>C	XM_011534636.3:c.1710+13581A>G	XM_011534636.3:c.1710+13581A>T
RANBP17 transcript variant X19	XM_011534637.3:c.1710+13581=	XM_011534637.3:c.1710+13581A>C	XM_011534637.3:c.1710+13581A>G	XM_011534637.3:c.1710+13581A>T
RANBP17 transcript variant X2	XM_017009736.2:c.1590+13581=	XM_017009736.2:c.1590+13581A>C	XM_017009736.2:c.1590+13581A>G	XM_017009736.2:c.1590+13581A>T
RANBP17 transcript variant X4	XM_017009738.2:c.1563+13581=	XM_017009738.2:c.1563+13581A>C	XM_017009738.2:c.1563+13581A>G	XM_017009738.2:c.1563+13581A>T
RANBP17 transcript variant X5	XM_017009739.2:c.1563+13581=	XM_017009739.2:c.1563+13581A>C	XM_017009739.2:c.1563+13581A>G	XM_017009739.2:c.1563+13581A>T
RANBP17 transcript variant X6	XM_017009740.2:c.1443+13581=	XM_017009740.2:c.1443+13581A>C	XM_017009740.2:c.1443+13581A>G	XM_017009740.2:c.1443+13581A>T
RANBP17 transcript variant X7	XM_017009741.3:c.1710+13581=	XM_017009741.3:c.1710+13581A>C	XM_017009741.3:c.1710+13581A>G	XM_017009741.3:c.1710+13581A>T
RANBP17 transcript variant X8	XM_017009742.3:c.1710+13581=	XM_017009742.3:c.1710+13581A>C	XM_017009742.3:c.1710+13581A>G	XM_017009742.3:c.1710+13581A>T
RANBP17 transcript variant X10	XM_017009744.2:c.1710+13581=	XM_017009744.2:c.1710+13581A>C	XM_017009744.2:c.1710+13581A>G	XM_017009744.2:c.1710+13581A>T
RANBP17 transcript variant X12	XM_017009745.2:c.810+13581=	XM_017009745.2:c.810+13581A>C	XM_017009745.2:c.810+13581A>G	XM_017009745.2:c.810+13581A>T
RANBP17 transcript variant X15	XM_017009746.3:c.1711-1107=	XM_017009746.3:c.1711-1107A>C	XM_017009746.3:c.1711-1107A>G	XM_017009746.3:c.1711-1107A>T
RANBP17 transcript variant X3	XM_047417530.1:c.1590+13581=	XM_047417530.1:c.1590+13581A>C	XM_047417530.1:c.1590+13581A>G	XM_047417530.1:c.1590+13581A>T
RANBP17 transcript variant X11	XM_047417531.1:c.1710+13581=	XM_047417531.1:c.1710+13581A>C	XM_047417531.1:c.1710+13581A>G	XM_047417531.1:c.1710+13581A>T
RANBP17 transcript variant X13	XM_047417532.1:c.1590+13581=	XM_047417532.1:c.1590+13581A>C	XM_047417532.1:c.1590+13581A>G	XM_047417532.1:c.1590+13581A>T
RANBP17 transcript variant X20	XM_047417533.1:c.159+13581=	XM_047417533.1:c.159+13581A>C	XM_047417533.1:c.159+13581A>G	XM_047417533.1:c.159+13581A>T

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

136 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss13884460	Dec 05, 2003 (119)
2	CSHL-HAPMAP	ss17056278	Feb 27, 2004 (120)
3	SSAHASNP	ss22269753	Apr 05, 2004 (121)
4	ABI	ss42615467	Mar 14, 2006 (126)
5	ILLUMINA	ss65788544	Oct 16, 2006 (127)
6	ILLUMINA	ss66865693	Dec 01, 2006 (127)
7	ILLUMINA	ss66936928	Dec 01, 2006 (127)
8	ILLUMINA	ss68075933	Dec 12, 2006 (127)
9	ILLUMINA	ss70461086	May 25, 2008 (130)
10	ILLUMINA	ss70981850	May 17, 2007 (127)
11	ILLUMINA	ss75701521	Dec 07, 2007 (129)
12	KRIBB_YJKIM	ss84893827	Dec 15, 2007 (130)
13	BCMHGSC_JDW	ss93334375	Mar 24, 2008 (129)
14	HUMANGENOME_JCVI	ss98666073	Feb 06, 2009 (130)
15	1000GENOMES	ss109623802	Jan 24, 2009 (130)
16	1000GENOMES	ss113661193	Jan 25, 2009 (130)
17	ENSEMBL	ss143967318	Dec 01, 2009 (131)
18	ILLUMINA	ss152548783	Dec 01, 2009 (131)
19	GMI	ss156336498	Dec 01, 2009 (131)
20	ILLUMINA	ss159105041	Dec 01, 2009 (131)
21	ILLUMINA	ss159854608	Dec 01, 2009 (131)
22	COMPLETE_GENOMICS	ss162889399	Jul 04, 2010 (132)
23	COMPLETE_GENOMICS	ss166233623	Jul 04, 2010 (132)
24	COMPLETE_GENOMICS	ss167364837	Jul 04, 2010 (132)
25	ILLUMINA	ss169550971	Jul 04, 2010 (132)
26	BUSHMAN	ss201206070	Jul 04, 2010 (132)
27	ILLUMINA	ss209082924	Jul 04, 2010 (132)
28	1000GENOMES	ss222116566	Jul 14, 2010 (132)
29	1000GENOMES	ss233256507	Jul 14, 2010 (132)
30	1000GENOMES	ss240357009	Jul 15, 2010 (132)
31	GMI	ss278586483	May 04, 2012 (137)
32	GMI	ss285309018	Apr 25, 2013 (138)
33	PJP	ss293520757	May 09, 2011 (134)
34	ILLUMINA	ss479164374	May 04, 2012 (137)
35	ILLUMINA	ss479166236	May 04, 2012 (137)
36	ILLUMINA	ss479484990	Sep 08, 2015 (146)
37	ILLUMINA	ss484383359	May 04, 2012 (137)
38	ILLUMINA	ss536568199	Sep 08, 2015 (146)
39	TISHKOFF	ss558888982	Apr 25, 2013 (138)
40	SSMP	ss652798954	Apr 25, 2013 (138)
41	ILLUMINA	ss778344743	Sep 08, 2015 (146)
42	ILLUMINA	ss782637975	Sep 08, 2015 (146)
43	ILLUMINA	ss783607480	Sep 08, 2015 (146)
44	ILLUMINA	ss831888110	Sep 08, 2015 (146)
45	ILLUMINA	ss832617833	Jul 13, 2019 (153)
46	ILLUMINA	ss833799384	Sep 08, 2015 (146)
47	EVA-GONL	ss982411383	Aug 21, 2014 (142)
48	JMKIDD_LAB	ss1073257241	Aug 21, 2014 (142)
49	1000GENOMES	ss1318325223	Aug 21, 2014 (142)
50	DDI	ss1430583097	Apr 01, 2015 (144)
51	EVA_GENOME_DK	ss1581462426	Apr 01, 2015 (144)
52	EVA_DECODE	ss1591953927	Apr 01, 2015 (144)
53	EVA_UK10K_ALSPAC	ss1614610842	Apr 01, 2015 (144)
54	EVA_UK10K_TWINSUK	ss1657604875	Apr 01, 2015 (144)
55	EVA_SVP	ss1712822027	Apr 01, 2015 (144)
56	ILLUMINA	ss1752563697	Sep 08, 2015 (146)
57	HAMMER_LAB	ss1804200823	Sep 08, 2015 (146)
58	WEILL_CORNELL_DGM	ss1925660958	Feb 12, 2016 (147)
59	ILLUMINA	ss1946163004	Feb 12, 2016 (147)
60	ILLUMINA	ss1958846218	Feb 12, 2016 (147)
61	GENOMED	ss1970271579	Jul 19, 2016 (147)
62	JJLAB	ss2023444122	Sep 14, 2016 (149)
63	USC_VALOUEV	ss2151604002	Dec 20, 2016 (150)
64	HUMAN_LONGEVITY	ss2280492188	Dec 20, 2016 (150)
65	SYSTEMSBIOZJU	ss2626210347	Nov 08, 2017 (151)
66	ILLUMINA	ss2634376074	Nov 08, 2017 (151)
67	GRF	ss2707180470	Nov 08, 2017 (151)
68	ILLUMINA	ss2711055224	Nov 08, 2017 (151)
69	GNOMAD	ss2833944077	Nov 08, 2017 (151)
70	SWEGEN	ss2998236473	Nov 08, 2017 (151)
71	ILLUMINA	ss3022556127	Nov 08, 2017 (151)
72	BIOINF_KMB_FNS_UNIBA	ss3025505089	Nov 08, 2017 (151)
73	CSHL	ss3346751853	Nov 08, 2017 (151)
74	ILLUMINA	ss3625889670	Oct 12, 2018 (152)
75	ILLUMINA	ss3629404021	Oct 12, 2018 (152)
76	ILLUMINA	ss3632297594	Oct 12, 2018 (152)
77	ILLUMINA	ss3633399698	Oct 12, 2018 (152)
78	ILLUMINA	ss3634121303	Oct 12, 2018 (152)
79	ILLUMINA	ss3635035774	Oct 12, 2018 (152)
80	ILLUMINA	ss3635802798	Oct 12, 2018 (152)
81	ILLUMINA	ss3636749584	Oct 12, 2018 (152)
82	ILLUMINA	ss3637555486	Oct 12, 2018 (152)
83	ILLUMINA	ss3638596727	Oct 12, 2018 (152)
84	ILLUMINA	ss3639301009	Oct 12, 2018 (152)
85	ILLUMINA	ss3639947241	Oct 12, 2018 (152)
86	ILLUMINA	ss3640743068	Oct 12, 2018 (152)
87	ILLUMINA	ss3641188514	Oct 12, 2018 (152)
88	ILLUMINA	ss3641485562	Oct 12, 2018 (152)
89	ILLUMINA	ss3643539339	Oct 12, 2018 (152)
90	ILLUMINA	ss3643992442	Oct 12, 2018 (152)
91	ILLUMINA	ss3644896061	Oct 12, 2018 (152)
92	URBANLAB	ss3648227897	Oct 12, 2018 (152)
93	ILLUMINA	ss3653062304	Oct 12, 2018 (152)
94	EGCUT_WGS	ss3666174120	Jul 13, 2019 (153)
95	EVA_DECODE	ss3716247390	Jul 13, 2019 (153)
96	ILLUMINA	ss3726294642	Jul 13, 2019 (153)
97	ACPOP	ss3733054386	Jul 13, 2019 (153)
98	ILLUMINA	ss3744263860	Jul 13, 2019 (153)
99	ILLUMINA	ss3745335933	Jul 13, 2019 (153)
100	EVA	ss3764407201	Jul 13, 2019 (153)
101	PAGE_CC	ss3771249820	Jul 13, 2019 (153)
102	ILLUMINA	ss3772829810	Jul 13, 2019 (153)
103	PACBIO	ss3785323989	Jul 13, 2019 (153)
104	PACBIO	ss3790695560	Jul 13, 2019 (153)
105	PACBIO	ss3795572690	Jul 13, 2019 (153)
106	KHV_HUMAN_GENOMES	ss3807569515	Jul 13, 2019 (153)
107	EVA	ss3829642300	Apr 26, 2020 (154)
108	EVA	ss3838294508	Apr 26, 2020 (154)
109	EVA	ss3843738404	Apr 26, 2020 (154)
110	HGDP	ss3847816605	Apr 26, 2020 (154)
111	SGDP_PRJ	ss3863551713	Apr 26, 2020 (154)
112	KRGDB	ss3910260456	Apr 26, 2020 (154)
113	KOGIC	ss3958167561	Apr 26, 2020 (154)
114	EVA	ss3984558687	Apr 26, 2021 (155)
115	EVA	ss3985188503	Apr 26, 2021 (155)
116	EVA	ss4017245992	Apr 26, 2021 (155)
117	TOPMED	ss4688394848	Apr 26, 2021 (155)
118	TOMMO_GENOMICS	ss5175395787	Apr 26, 2021 (155)
119	1000G_HIGH_COVERAGE	ss5266812428	Oct 13, 2022 (156)
120	GENOGRAPHIC	ss5314510683	Oct 13, 2022 (156)
121	EVA	ss5315107125	Oct 13, 2022 (156)
122	EVA	ss5362761429	Oct 13, 2022 (156)
123	HUGCELL_USP	ss5464682309	Oct 13, 2022 (156)
124	EVA	ss5508306139	Oct 13, 2022 (156)
125	1000G_HIGH_COVERAGE	ss5551968251	Oct 13, 2022 (156)
126	SANFORD_IMAGENETICS	ss5624609364	Oct 13, 2022 (156)
127	SANFORD_IMAGENETICS	ss5639430546	Oct 13, 2022 (156)
128	TOMMO_GENOMICS	ss5712833465	Oct 13, 2022 (156)
129	EVA	ss5799670454	Oct 13, 2022 (156)
130	YY_MCH	ss5807002322	Oct 13, 2022 (156)
131	EVA	ss5836021445	Oct 13, 2022 (156)
132	EVA	ss5847279861	Oct 13, 2022 (156)
133	EVA	ss5855130749	Oct 13, 2022 (156)
134	EVA	ss5897451908	Oct 13, 2022 (156)
135	EVA	ss5967930052	Oct 13, 2022 (156)
136	EVA	ss5979763730	Oct 13, 2022 (156)
137	1000Genomes	NC_000005.9 - 170408962	Oct 12, 2018 (152)
138	1000Genomes_30x	NC_000005.10 - 170981958	Oct 13, 2022 (156)
139	The Avon Longitudinal Study of Parents and Children	NC_000005.9 - 170408962	Oct 12, 2018 (152)
140	Genetic variation in the Estonian population	NC_000005.9 - 170408962	Oct 12, 2018 (152)
141	Genographic Project	NC_000005.10 - 170981958	Oct 13, 2022 (156)
142	The Danish reference pan genome	NC_000005.9 - 170408962	Apr 26, 2020 (154)
143	gnomAD - Genomes	NC_000005.10 - 170981958	Apr 26, 2021 (155)
144	Genome of the Netherlands Release 5	NC_000005.9 - 170408962	Apr 26, 2020 (154)
145	HGDP-CEPH-db Supplement 1	NC_000005.8 - 170341567	Apr 26, 2020 (154)
146	HapMap	NC_000005.10 - 170981958	Apr 26, 2020 (154)
147	KOREAN population from KRGDB	NC_000005.9 - 170408962	Apr 26, 2020 (154)
148	Korean Genome Project	NC_000005.10 - 170981958	Apr 26, 2020 (154)
149	Northern Sweden	NC_000005.9 - 170408962	Jul 13, 2019 (153)
150	The PAGE Study	NC_000005.10 - 170981958	Jul 13, 2019 (153)
151	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000005.9 - 170408962	Apr 26, 2021 (155)
152	CNV burdens in cranial meningiomas	NC_000005.9 - 170408962	Apr 26, 2021 (155)
153	Qatari	NC_000005.9 - 170408962	Apr 26, 2020 (154)
154	SGDP_PRJ	NC_000005.9 - 170408962	Apr 26, 2020 (154)
155	Siberian	NC_000005.9 - 170408962	Apr 26, 2020 (154)
156	8.3KJPN	NC_000005.9 - 170408962	Apr 26, 2021 (155)
157	14KJPN	NC_000005.10 - 170981958	Oct 13, 2022 (156)
158	TopMed	NC_000005.10 - 170981958	Apr 26, 2021 (155)
159	UK 10K study - Twins	NC_000005.9 - 170408962	Oct 12, 2018 (152)
160	A Vietnamese Genetic Variation Database	NC_000005.9 - 170408962	Jul 13, 2019 (153)
161	ALFA	NC_000005.10 - 170981958	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs60206439	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
17437850, ss3910260456	NC_000005.9:170408961:A:C	NC_000005.10:170981957:A:C	(self)
494497, ss93334375, ss109623802, ss113661193, ss162889399, ss166233623, ss167364837, ss201206070, ss278586483, ss285309018, ss293520757, ss479164374, ss1591953927, ss1712822027, ss3639301009, ss3639947241, ss3643539339, ss3643992442, ss3847816605	NC_000005.8:170341566:A:G	NC_000005.10:170981957:A:G	(self)
30042978, 16726684, 11912368, 7627365, 7423803, 17437850, 6339251, 414430, 108061, 7702888, 15568693, 4120356, 33365094, 16726684, 3706845, ss222116566, ss233256507, ss240357009, ss479166236, ss479484990, ss484383359, ss536568199, ss558888982, ss652798954, ss778344743, ss782637975, ss783607480, ss831888110, ss832617833, ss833799384, ss982411383, ss1073257241, ss1318325223, ss1430583097, ss1581462426, ss1614610842, ss1657604875, ss1752563697, ss1804200823, ss1925660958, ss1946163004, ss1958846218, ss1970271579, ss2023444122, ss2151604002, ss2626210347, ss2634376074, ss2707180470, ss2711055224, ss2833944077, ss2998236473, ss3022556127, ss3346751853, ss3625889670, ss3629404021, ss3632297594, ss3633399698, ss3634121303, ss3635035774, ss3635802798, ss3636749584, ss3637555486, ss3638596727, ss3640743068, ss3641188514, ss3641485562, ss3644896061, ss3653062304, ss3666174120, ss3733054386, ss3744263860, ss3745335933, ss3764407201, ss3772829810, ss3785323989, ss3790695560, ss3795572690, ss3829642300, ss3838294508, ss3863551713, ss3910260456, ss3984558687, ss3985188503, ss4017245992, ss5175395787, ss5315107125, ss5362761429, ss5508306139, ss5624609364, ss5639430546, ss5799670454, ss5836021445, ss5847279861, ss5967930052, ss5979763730	NC_000005.9:170408961:A:G	NC_000005.10:170981957:A:G	(self)
39494186, 47291, 212486807, 3026543, 14545562, 471289, 46670569, 525772405, 4892533130, ss2280492188, ss3025505089, ss3648227897, ss3716247390, ss3726294642, ss3771249820, ss3807569515, ss3843738404, ss3958167561, ss4688394848, ss5266812428, ss5314510683, ss5464682309, ss5551968251, ss5712833465, ss5807002322, ss5855130749, ss5897451908	NC_000005.10:170981957:A:G	NC_000005.10:170981957:A:G	(self)
ss13884460, ss17056278, ss22269753	NT_023133.11:15218546:A:G	NC_000005.10:170981957:A:G	(self)
ss42615467, ss65788544, ss66865693, ss66936928, ss68075933, ss70461086, ss70981850, ss75701521, ss84893827, ss98666073, ss143967318, ss152548783, ss156336498, ss159105041, ss159854608, ss169550971, ss209082924	NT_023133.13:15220234:A:G	NC_000005.10:170981957:A:G	(self)
17437850, ss3910260456	NC_000005.9:170408961:A:T	NC_000005.10:170981957:A:T	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs10037007

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs10037007