Name: rs150
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.

rs150

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:24971033 (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: C>A / C>G / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.142559 (37734/264690, TOPMED)
C=0.153702 (21553/140226, GnomAD)
C=0.22825 (6450/28258, 14KJPN) (+ 17 more)
C=0.16024 (3457/21574, ALFA)
C=0.22622 (3791/16758, 8.3KJPN)
C=0.1141 (731/6404, 1000G_30x)
C=0.1198 (600/5008, 1000G)
C=0.1938 (868/4480, Estonian)
C=0.2252 (868/3854, ALSPAC)
C=0.2125 (788/3708, TWINSUK)
C=0.1672 (490/2930, KOREAN)
C=0.1736 (318/1832, Korea1K)
C=0.227 (227/998, GoNL)
C=0.217 (130/600, NorthernSweden)
C=0.093 (51/546, SGDP_PRJ)
C=0.102 (22/216, Qatari)
C=0.107 (23/214, Vietnamese)
C=0.255 (53/208, HapMap)
C=0.13 (7/54, Siberian)
C=0.35 (14/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: OSBPL3 : 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	21574	C=0.16024	T=0.83976
European	Sub	14286	C=0.20496	T=0.79504
African	Sub	5578	C=0.0520	T=0.9480
African Others	Sub	198	C=0.051	T=0.949
African American	Sub	5380	C=0.0520	T=0.9480
Asian	Sub	112	C=0.143	T=0.857
East Asian	Sub	86	C=0.19	T=0.81
Other Asian	Sub	26	C=0.00	T=1.00
Latin American 1	Sub	146	C=0.137	T=0.863
Latin American 2	Sub	610	C=0.152	T=0.848
South Asian	Sub	98	C=0.10	T=0.90
Other	Sub	744	C=0.134	T=0.866

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	C=0.142559	T=0.857441
gnomAD - Genomes	Global	Study-wide	140226	C=0.153702	T=0.846298
gnomAD - Genomes	European	Sub	75924	C=0.21277	T=0.78723
gnomAD - Genomes	African	Sub	42038	C=0.05264	T=0.94736
gnomAD - Genomes	American	Sub	13660	C=0.13111	T=0.86889
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	C=0.1979	T=0.8021
gnomAD - Genomes	East Asian	Sub	3132	C=0.1360	T=0.8640
gnomAD - Genomes	Other	Sub	2152	C=0.1450	T=0.8550
14KJPN	JAPANESE	Study-wide	28258	C=0.22825	T=0.77175
Allele Frequency Aggregator	Total	Global	21574	C=0.16024	T=0.83976
Allele Frequency Aggregator	European	Sub	14286	C=0.20496	T=0.79504
Allele Frequency Aggregator	African	Sub	5578	C=0.0520	T=0.9480
Allele Frequency Aggregator	Other	Sub	744	C=0.134	T=0.866
Allele Frequency Aggregator	Latin American 2	Sub	610	C=0.152	T=0.848
Allele Frequency Aggregator	Latin American 1	Sub	146	C=0.137	T=0.863
Allele Frequency Aggregator	Asian	Sub	112	C=0.143	T=0.857
Allele Frequency Aggregator	South Asian	Sub	98	C=0.10	T=0.90
8.3KJPN	JAPANESE	Study-wide	16758	C=0.22622	T=0.77378
1000Genomes_30x	Global	Study-wide	6404	C=0.1141	T=0.8859
1000Genomes_30x	African	Sub	1786	C=0.0274	T=0.9726
1000Genomes_30x	Europe	Sub	1266	C=0.2227	T=0.7773
1000Genomes_30x	South Asian	Sub	1202	C=0.0732	T=0.9268
1000Genomes_30x	East Asian	Sub	1170	C=0.1598	T=0.8402
1000Genomes_30x	American	Sub	980	C=0.128	T=0.872
1000Genomes	Global	Study-wide	5008	C=0.1198	T=0.8802
1000Genomes	African	Sub	1322	C=0.0310	T=0.9690
1000Genomes	East Asian	Sub	1008	C=0.1587	T=0.8413
1000Genomes	Europe	Sub	1006	C=0.2256	T=0.7744
1000Genomes	South Asian	Sub	978	C=0.079	T=0.921
1000Genomes	American	Sub	694	C=0.137	T=0.863
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.1938	T=0.8063
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.2252	T=0.7748
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.2125	T=0.7875
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.1672	A=0.0000, G=0.0000, T=0.8328
Korean Genome Project	KOREAN	Study-wide	1832	C=0.1736	T=0.8264
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.227	T=0.773
Northern Sweden	ACPOP	Study-wide	600	C=0.217	T=0.783
SGDP_PRJ	Global	Study-wide	546	C=0.093	T=0.907
Qatari	Global	Study-wide	216	C=0.102	T=0.898
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.107	T=0.893
HapMap	Global	Study-wide	208	C=0.255	T=0.745
HapMap	American	Sub	120	C=0.283	T=0.717
HapMap	Asian	Sub	88	C=0.22	T=0.78
Siberian	Global	Study-wide	54	C=0.13	T=0.87
The Danish reference pan genome	Danish	Study-wide	40	C=0.35	T=0.65

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 7	NC_000007.14:g.24971033C>A
GRCh38.p14 chr 7	NC_000007.14:g.24971033C>G
GRCh38.p14 chr 7	NC_000007.14:g.24971033C>T
GRCh37.p13 chr 7	NC_000007.13:g.25010652C>A
GRCh37.p13 chr 7	NC_000007.13:g.25010652C>G
GRCh37.p13 chr 7	NC_000007.13:g.25010652C>T

Gene: OSBPL3, oxysterol binding protein like 3 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
OSBPL3 transcript variant 1	NM_015550.4:c.-150+8853G>T	N/A	Intron Variant
OSBPL3 transcript variant 2	NM_145320.2:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant 3	NM_145321.2:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant 4	NM_145322.2:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant 5	NR_104111.1:n.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant 6	NR_104112.1:n.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant X17	XM_006715681.4:c.-150+885… XM_006715681.4:c.-150+8853G>T	N/A	Intron Variant
OSBPL3 transcript variant X22	XM_006715682.4:c.-150+885… XM_006715682.4:c.-150+8853G>T	N/A	Intron Variant
OSBPL3 transcript variant X27	XM_006715683.4:c.-150+885… XM_006715683.4:c.-150+8853G>T	N/A	Intron Variant
OSBPL3 transcript variant X1	XM_047420129.1:c.-150+885… XM_047420129.1:c.-150+8853G>T	N/A	Intron Variant
OSBPL3 transcript variant X3	XM_047420131.1:c.-150+104… XM_047420131.1:c.-150+10497G>T	N/A	Intron Variant
OSBPL3 transcript variant X6	XM_047420134.1:c.-150+104… XM_047420134.1:c.-150+10497G>T	N/A	Intron Variant
OSBPL3 transcript variant X9	XM_047420135.1:c.-150+927… XM_047420135.1:c.-150+9273G>T	N/A	Intron Variant
OSBPL3 transcript variant X10	XM_047420136.1:c.-150+847… XM_047420136.1:c.-150+8477G>T	N/A	Intron Variant
OSBPL3 transcript variant X11	XM_047420137.1:c.-150+103… XM_047420137.1:c.-150+10366G>T	N/A	Intron Variant
OSBPL3 transcript variant X13	XM_047420139.1:c.-150+885… XM_047420139.1:c.-150+8853G>T	N/A	Intron Variant
OSBPL3 transcript variant X16	XM_047420142.1:c.-150+885… XM_047420142.1:c.-150+8853G>T	N/A	Intron Variant
OSBPL3 transcript variant X20	XM_047420145.1:c.-150+103… XM_047420145.1:c.-150+10366G>T	N/A	Intron Variant
OSBPL3 transcript variant X21	XM_047420146.1:c.-150+104… XM_047420146.1:c.-150+10497G>T	N/A	Intron Variant
OSBPL3 transcript variant X24	XM_047420148.1:c.-150+103… XM_047420148.1:c.-150+10371G>T	N/A	Intron Variant
OSBPL3 transcript variant X29	XM_047420152.1:c.-150+885… XM_047420152.1:c.-150+8853G>T	N/A	Intron Variant
OSBPL3 transcript variant X7	XM_005249698.4:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant X8	XM_011515258.3:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant X2	XM_047420130.1:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant X4	XM_047420132.1:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant X5	XM_047420133.1:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant X12	XM_047420138.1:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant X14	XM_047420140.1:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant X15	XM_047420141.1:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant X18	XM_047420143.1:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant X19	XM_047420144.1:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant X23	XM_047420147.1:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant X25	XM_047420149.1:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant X26	XM_047420150.1:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant X28	XM_047420151.1:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant X37	XM_047420153.1:c.	N/A	Genic Upstream Transcript Variant
OSBPL3 transcript variant X30	XR_007060001.1:n.	N/A	Intron Variant
OSBPL3 transcript variant X31	XR_007060002.1:n.	N/A	Intron Variant
OSBPL3 transcript variant X33	XR_007060004.1:n.	N/A	Intron Variant
OSBPL3 transcript variant X34	XR_007060005.1:n.	N/A	Intron Variant
OSBPL3 transcript variant X35	XR_007060006.1:n.	N/A	Intron Variant
OSBPL3 transcript variant X36	XR_007060007.1:n.	N/A	Intron Variant
OSBPL3 transcript variant X32	XR_007060003.1:n.	N/A	Genic Upstream Transcript 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	C=	A	G	T
GRCh38.p14 chr 7	NC_000007.14:g.24971033=	NC_000007.14:g.24971033C>A	NC_000007.14:g.24971033C>G	NC_000007.14:g.24971033C>T
GRCh37.p13 chr 7	NC_000007.13:g.25010652=	NC_000007.13:g.25010652C>A	NC_000007.13:g.25010652C>G	NC_000007.13:g.25010652C>T
OSBPL3 transcript variant 1	NM_015550.2:c.-150+8853=	NM_015550.2:c.-150+8853G>T	NM_015550.2:c.-150+8853G>C	NM_015550.2:c.-150+8853G>A
OSBPL3 transcript variant 1	NM_015550.4:c.-150+8853=	NM_015550.4:c.-150+8853G>T	NM_015550.4:c.-150+8853G>C	NM_015550.4:c.-150+8853G>A
OSBPL3 transcript variant 2	NM_145320.1:c.-150+8853=	NM_145320.1:c.-150+8853G>T	NM_145320.1:c.-150+8853G>C	NM_145320.1:c.-150+8853G>A
OSBPL3 transcript variant 3	NM_145321.1:c.-150+8853=	NM_145321.1:c.-150+8853G>T	NM_145321.1:c.-150+8853G>C	NM_145321.1:c.-150+8853G>A
OSBPL3 transcript variant 4	NM_145322.1:c.-150+8853=	NM_145322.1:c.-150+8853G>T	NM_145322.1:c.-150+8853G>C	NM_145322.1:c.-150+8853G>A
OSBPL3 transcript variant X17	XM_006715681.4:c.-150+8853=	XM_006715681.4:c.-150+8853G>T	XM_006715681.4:c.-150+8853G>C	XM_006715681.4:c.-150+8853G>A
OSBPL3 transcript variant X22	XM_006715682.4:c.-150+8853=	XM_006715682.4:c.-150+8853G>T	XM_006715682.4:c.-150+8853G>C	XM_006715682.4:c.-150+8853G>A
OSBPL3 transcript variant X27	XM_006715683.4:c.-150+8853=	XM_006715683.4:c.-150+8853G>T	XM_006715683.4:c.-150+8853G>C	XM_006715683.4:c.-150+8853G>A
OSBPL3 transcript variant X1	XM_047420129.1:c.-150+8853=	XM_047420129.1:c.-150+8853G>T	XM_047420129.1:c.-150+8853G>C	XM_047420129.1:c.-150+8853G>A
OSBPL3 transcript variant X3	XM_047420131.1:c.-150+10497=	XM_047420131.1:c.-150+10497G>T	XM_047420131.1:c.-150+10497G>C	XM_047420131.1:c.-150+10497G>A
OSBPL3 transcript variant X6	XM_047420134.1:c.-150+10497=	XM_047420134.1:c.-150+10497G>T	XM_047420134.1:c.-150+10497G>C	XM_047420134.1:c.-150+10497G>A
OSBPL3 transcript variant X9	XM_047420135.1:c.-150+9273=	XM_047420135.1:c.-150+9273G>T	XM_047420135.1:c.-150+9273G>C	XM_047420135.1:c.-150+9273G>A
OSBPL3 transcript variant X10	XM_047420136.1:c.-150+8477=	XM_047420136.1:c.-150+8477G>T	XM_047420136.1:c.-150+8477G>C	XM_047420136.1:c.-150+8477G>A
OSBPL3 transcript variant X11	XM_047420137.1:c.-150+10366=	XM_047420137.1:c.-150+10366G>T	XM_047420137.1:c.-150+10366G>C	XM_047420137.1:c.-150+10366G>A
OSBPL3 transcript variant X13	XM_047420139.1:c.-150+8853=	XM_047420139.1:c.-150+8853G>T	XM_047420139.1:c.-150+8853G>C	XM_047420139.1:c.-150+8853G>A
OSBPL3 transcript variant X16	XM_047420142.1:c.-150+8853=	XM_047420142.1:c.-150+8853G>T	XM_047420142.1:c.-150+8853G>C	XM_047420142.1:c.-150+8853G>A
OSBPL3 transcript variant X20	XM_047420145.1:c.-150+10366=	XM_047420145.1:c.-150+10366G>T	XM_047420145.1:c.-150+10366G>C	XM_047420145.1:c.-150+10366G>A
OSBPL3 transcript variant X21	XM_047420146.1:c.-150+10497=	XM_047420146.1:c.-150+10497G>T	XM_047420146.1:c.-150+10497G>C	XM_047420146.1:c.-150+10497G>A
OSBPL3 transcript variant X24	XM_047420148.1:c.-150+10371=	XM_047420148.1:c.-150+10371G>T	XM_047420148.1:c.-150+10371G>C	XM_047420148.1:c.-150+10371G>A
OSBPL3 transcript variant X29	XM_047420152.1:c.-150+8853=	XM_047420152.1:c.-150+8853G>T	XM_047420152.1:c.-150+8853G>C	XM_047420152.1:c.-150+8853G>A

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#.

84 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	KWOK	ss150	Sep 19, 2000 (36)
2	SC_JCM	ss3535333	Sep 28, 2001 (100)
3	BCM_SSAHASNP	ss10396733	Jul 11, 2003 (116)
4	WUGSC_SSAHASNP	ss14567547	Dec 05, 2003 (120)
5	CSHL-HAPMAP	ss20313692	Feb 27, 2004 (120)
6	SSAHASNP	ss22528067	Apr 05, 2004 (121)
7	SSAHASNP	ss22901432	Apr 05, 2004 (121)
8	PERLEGEN	ss24423211	Sep 20, 2004 (123)
9	ABI	ss44794280	Mar 14, 2006 (126)
10	HGSV	ss80754202	Dec 15, 2007 (130)
11	HGSV	ss84499336	Dec 15, 2007 (130)
12	HGSV	ss85836773	Dec 15, 2007 (130)
13	BCMHGSC_JDW	ss93646313	Mar 24, 2008 (129)
14	HUMANGENOME_JCVI	ss98139973	Feb 05, 2009 (130)
15	BGI	ss105507371	Feb 05, 2009 (130)
16	1000GENOMES	ss111691829	Jan 25, 2009 (130)
17	1000GENOMES	ss113478260	Jan 25, 2009 (130)
18	ILLUMINA-UK	ss115987783	Feb 14, 2009 (130)
19	ENSEMBL	ss142760778	Dec 01, 2009 (131)
20	ENSEMBL	ss144059685	Dec 01, 2009 (131)
21	GMI	ss154529273	Dec 01, 2009 (131)
22	COMPLETE_GENOMICS	ss162141896	Jul 04, 2010 (132)
23	COMPLETE_GENOMICS	ss163848341	Jul 04, 2010 (132)
24	COMPLETE_GENOMICS	ss166295438	Jul 04, 2010 (132)
25	BUSHMAN	ss203089834	Jul 04, 2010 (132)
26	BCM-HGSC-SUB	ss207940782	Jul 04, 2010 (132)
27	1000GENOMES	ss222968839	Jul 14, 2010 (132)
28	1000GENOMES	ss233894584	Jul 15, 2010 (132)
29	1000GENOMES	ss240866080	Jul 15, 2010 (132)
30	BL	ss254128295	May 09, 2011 (134)
31	GMI	ss279229211	May 04, 2012 (137)
32	GMI	ss285592417	Apr 25, 2013 (138)
33	PJP	ss294032316	May 09, 2011 (134)
34	TISHKOFF	ss559875911	Apr 25, 2013 (138)
35	SSMP	ss654229256	Apr 25, 2013 (138)
36	EVA-GONL	ss984064469	Aug 21, 2014 (142)
37	JMKIDD_LAB	ss1074451646	Aug 21, 2014 (142)
38	1000GENOMES	ss1324347510	Aug 21, 2014 (142)
39	DDI	ss1431061325	Apr 01, 2015 (144)
40	EVA_GENOME_DK	ss1582116815	Apr 01, 2015 (144)
41	EVA_DECODE	ss1593633337	Apr 01, 2015 (144)
42	EVA_UK10K_ALSPAC	ss1617794981	Apr 01, 2015 (144)
43	EVA_UK10K_TWINSUK	ss1660789014	Apr 01, 2015 (144)
44	HAMMER_LAB	ss1804916960	Sep 08, 2015 (146)
45	WEILL_CORNELL_DGM	ss1927309479	Feb 12, 2016 (147)
46	GENOMED	ss1970651681	Jul 19, 2016 (147)
47	JJLAB	ss2024331893	Sep 14, 2016 (149)
48	USC_VALOUEV	ss2152527977	Dec 20, 2016 (150)
49	HUMAN_LONGEVITY	ss2292529051	Dec 20, 2016 (150)
50	SYSTEMSBIOZJU	ss2626654871	Nov 08, 2017 (151)
51	GRF	ss2708184802	Nov 08, 2017 (151)
52	GNOMAD	ss2850933165	Nov 08, 2017 (151)
53	SWEGEN	ss3000794696	Nov 08, 2017 (151)
54	BIOINF_KMB_FNS_UNIBA	ss3025960214	Nov 08, 2017 (151)
55	CSHL	ss3347488421	Nov 08, 2017 (151)
56	URBANLAB	ss3648585869	Oct 12, 2018 (152)
57	EGCUT_WGS	ss3668723503	Jul 13, 2019 (153)
58	EVA_DECODE	ss3719305125	Jul 13, 2019 (153)
59	ACPOP	ss3734452171	Jul 13, 2019 (153)
60	EVA	ss3766317199	Jul 13, 2019 (153)
61	PACBIO	ss3785760810	Jul 13, 2019 (153)
62	PACBIO	ss3791071237	Jul 13, 2019 (153)
63	PACBIO	ss3795950992	Jul 13, 2019 (153)
64	KHV_HUMAN_GENOMES	ss3809484657	Jul 13, 2019 (153)
65	EVA	ss3830470711	Apr 26, 2020 (154)
66	EVA	ss3838722647	Apr 26, 2020 (154)
67	EVA	ss3844173903	Apr 26, 2020 (154)
68	SGDP_PRJ	ss3866853940	Apr 26, 2020 (154)
69	KRGDB	ss3913892196	Apr 26, 2020 (154)
70	KOGIC	ss3961078262	Apr 26, 2020 (154)
71	TOPMED	ss4739191533	Apr 26, 2021 (155)
72	TOMMO_GENOMICS	ss5182270968	Apr 26, 2021 (155)
73	1000G_HIGH_COVERAGE	ss5272193768	Oct 14, 2022 (156)
74	EVA	ss5372309579	Oct 14, 2022 (156)
75	HUGCELL_USP	ss5469442224	Oct 14, 2022 (156)
76	EVA	ss5508885905	Oct 14, 2022 (156)
77	1000G_HIGH_COVERAGE	ss5560019535	Oct 14, 2022 (156)
78	SANFORD_IMAGENETICS	ss5642557152	Oct 14, 2022 (156)
79	TOMMO_GENOMICS	ss5721853641	Oct 14, 2022 (156)
80	YY_MCH	ss5808427901	Oct 14, 2022 (156)
81	EVA	ss5822551593	Oct 14, 2022 (156)
82	EVA	ss5855809536	Oct 14, 2022 (156)
83	EVA	ss5858124971	Oct 14, 2022 (156)
84	EVA	ss5971757776	Oct 14, 2022 (156)
85	1000Genomes	NC_000007.13 - 25010652	Oct 12, 2018 (152)
86	1000Genomes_30x	NC_000007.14 - 24971033	Oct 14, 2022 (156)
87	The Avon Longitudinal Study of Parents and Children	NC_000007.13 - 25010652	Oct 12, 2018 (152)
88	Genetic variation in the Estonian population	NC_000007.13 - 25010652	Oct 12, 2018 (152)
89	The Danish reference pan genome	NC_000007.13 - 25010652	Apr 26, 2020 (154)
90	gnomAD - Genomes	NC_000007.14 - 24971033	Apr 26, 2021 (155)
91	Genome of the Netherlands Release 5	NC_000007.13 - 25010652	Apr 26, 2020 (154)
92	HapMap	NC_000007.14 - 24971033	Apr 26, 2020 (154)
93	KOREAN population from KRGDB	NC_000007.13 - 25010652	Apr 26, 2020 (154)
94	Korean Genome Project	NC_000007.14 - 24971033	Apr 26, 2020 (154)
95	Northern Sweden	NC_000007.13 - 25010652	Jul 13, 2019 (153)
96	Qatari	NC_000007.13 - 25010652	Apr 26, 2020 (154)
97	SGDP_PRJ	NC_000007.13 - 25010652	Apr 26, 2020 (154)
98	Siberian	NC_000007.13 - 25010652	Apr 26, 2020 (154)
99	8.3KJPN	NC_000007.13 - 25010652	Apr 26, 2021 (155)
100	14KJPN	NC_000007.14 - 24971033	Oct 14, 2022 (156)
101	TopMed	NC_000007.14 - 24971033	Apr 26, 2021 (155)
102	UK 10K study - Twins	NC_000007.13 - 25010652	Oct 12, 2018 (152)
103	A Vietnamese Genetic Variation Database	NC_000007.13 - 25010652	Jul 13, 2019 (153)
104	ALFA	NC_000007.14 - 24971033	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)
rs10362143	Feb 27, 2004 (120)
rs17297235	Oct 08, 2004 (123)
rs59577098	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
21069590, ss3913892196	NC_000007.13:25010651:C:A	NC_000007.14:24971032:C:A	(self)
21069590, ss3913892196	NC_000007.13:25010651:C:G	NC_000007.14:24971032:C:G	(self)
ss80754202, ss84499336, ss85836773	NC_000007.11:24783891:C:T	NC_000007.14:24971032:C:T	(self)
ss93646313, ss111691829, ss113478260, ss115987783, ss162141896, ss163848341, ss166295438, ss203089834, ss207940782, ss254128295, ss279229211, ss285592417, ss294032316, ss1593633337	NC_000007.12:24977176:C:T	NC_000007.14:24971032:C:T	(self)
36289524, 20230980, 14461751, 8281754, 9020114, 21069590, 7737036, 9351409, 18870920, 5044331, 40240275, 20230980, 4507767, ss222968839, ss233894584, ss240866080, ss559875911, ss654229256, ss984064469, ss1074451646, ss1324347510, ss1431061325, ss1582116815, ss1617794981, ss1660789014, ss1804916960, ss1927309479, ss1970651681, ss2024331893, ss2152527977, ss2626654871, ss2708184802, ss2850933165, ss3000794696, ss3347488421, ss3668723503, ss3734452171, ss3766317199, ss3785760810, ss3791071237, ss3795950992, ss3830470711, ss3838722647, ss3866853940, ss3913892196, ss5182270968, ss5372309579, ss5508885905, ss5642557152, ss5822551593, ss5971757776	NC_000007.13:25010651:C:T	NC_000007.14:24971032:C:T	(self)
47545470, 255882012, 3358922, 17456263, 55690745, 576569092, 11470298688, ss2292529051, ss3025960214, ss3648585869, ss3719305125, ss3809484657, ss3844173903, ss3961078262, ss4739191533, ss5272193768, ss5469442224, ss5560019535, ss5721853641, ss5808427901, ss5855809536, ss5858124971	NC_000007.14:24971032:C:T	NC_000007.14:24971032:C:T	(self)
ss10396733	NT_007819.13:24304259:C:T	NC_000007.14:24971032:C:T	(self)
ss14567547, ss20313692, ss22528067, ss22901432	NT_007819.14:24304259:C:T	NC_000007.14:24971032:C:T	(self)
ss150, ss3535333, ss24423211, ss44794280, ss98139973, ss105507371, ss142760778, ss144059685, ss154529273	NT_007819.17:25000651:C:T	NC_000007.14:24971032:C: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 rs150

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
Top▲ Help
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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs150