Name: rs10752275
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.

rs10752275

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:12758716 (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: G>A / G>C / G>T
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.156130 (41326/264690, TOPMED)
A=0.150182 (21045/140130, GnomAD)
A=0.13419 (5041/37566, ALFA) (+ 19 more)
A=0.31980 (9037/28258, 14KJPN)
A=0.32237 (5403/16760, 8.3KJPN)
A=0.2042 (1308/6404, 1000G_30x)
A=0.2087 (1045/5008, 1000G)
A=0.1857 (832/4480, Estonian)
A=0.0908 (350/3854, ALSPAC)
A=0.0777 (288/3708, TWINSUK)
A=0.3555 (1041/2928, KOREAN)
A=0.2332 (486/2084, HGDP_Stanford)
A=0.092 (92/998, GoNL)
A=0.241 (151/626, Chileans)
A=0.127 (76/600, NorthernSweden)
A=0.199 (43/216, Qatari)
A=0.301 (65/216, Vietnamese)
G=0.438 (91/208, SGDP_PRJ)
A=0.05 (2/40, GENOME_DK)
G=0.50 (6/12, Siberian)
A=0.50 (6/12, Siberian)
A=0.0 (0/10, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CAMK1D : 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	37566	G=0.86581	A=0.13419
European	Sub	27806	G=0.88725	A=0.11275
African	Sub	3838	G=0.8012	A=0.1988
African Others	Sub	136	G=0.765	A=0.235
African American	Sub	3702	G=0.8025	A=0.1975
Asian	Sub	176	G=0.642	A=0.358
East Asian	Sub	116	G=0.621	A=0.379
Other Asian	Sub	60	G=0.68	A=0.32
Latin American 1	Sub	312	G=0.837	A=0.163
Latin American 2	Sub	2812	G=0.7710	A=0.2290
South Asian	Sub	126	G=0.865	A=0.135
Other	Sub	2496	G=0.8526	A=0.1474

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
TopMed	Global	Study-wide	264690	G=0.843870	A=0.156130
gnomAD - Genomes	Global	Study-wide	140130	G=0.849818	A=0.150182
gnomAD - Genomes	European	Sub	75906	G=0.88882	A=0.11118
gnomAD - Genomes	African	Sub	41982	G=0.80744	A=0.19256
gnomAD - Genomes	American	Sub	13644	G=0.79999	A=0.20001
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	G=0.8700	A=0.1300
gnomAD - Genomes	East Asian	Sub	3122	G=0.6682	A=0.3318
gnomAD - Genomes	Other	Sub	2152	G=0.8490	A=0.1510
Allele Frequency Aggregator	Total	Global	37566	G=0.86581	A=0.13419
Allele Frequency Aggregator	European	Sub	27806	G=0.88725	A=0.11275
Allele Frequency Aggregator	African	Sub	3838	G=0.8012	A=0.1988
Allele Frequency Aggregator	Latin American 2	Sub	2812	G=0.7710	A=0.2290
Allele Frequency Aggregator	Other	Sub	2496	G=0.8526	A=0.1474
Allele Frequency Aggregator	Latin American 1	Sub	312	G=0.837	A=0.163
Allele Frequency Aggregator	Asian	Sub	176	G=0.642	A=0.358
Allele Frequency Aggregator	South Asian	Sub	126	G=0.865	A=0.135
14KJPN	JAPANESE	Study-wide	28258	G=0.68020	A=0.31980
8.3KJPN	JAPANESE	Study-wide	16760	G=0.67763	A=0.32237
1000Genomes_30x	Global	Study-wide	6404	G=0.7958	A=0.2042
1000Genomes_30x	African	Sub	1786	G=0.8085	A=0.1915
1000Genomes_30x	Europe	Sub	1266	G=0.8902	A=0.1098
1000Genomes_30x	South Asian	Sub	1202	G=0.8195	A=0.1805
1000Genomes_30x	East Asian	Sub	1170	G=0.6761	A=0.3239
1000Genomes_30x	American	Sub	980	G=0.764	A=0.236
1000Genomes	Global	Study-wide	5008	G=0.7913	A=0.2087
1000Genomes	African	Sub	1322	G=0.8018	A=0.1982
1000Genomes	East Asian	Sub	1008	G=0.6716	A=0.3284
1000Genomes	Europe	Sub	1006	G=0.8887	A=0.1113
1000Genomes	South Asian	Sub	978	G=0.823	A=0.177
1000Genomes	American	Sub	694	G=0.759	A=0.241
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.8143	A=0.1857
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.9092	A=0.0908
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.9223	A=0.0777
KOREAN population from KRGDB	KOREAN	Study-wide	2928	G=0.6445	A=0.3555, C=0.0000
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	G=0.7668	A=0.2332
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	G=0.683	A=0.317
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	G=0.804	A=0.196
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	G=0.826	A=0.174
HGDP-CEPH-db Supplement 1	Europe	Sub	320	G=0.869	A=0.131
HGDP-CEPH-db Supplement 1	Africa	Sub	242	G=0.814	A=0.186
HGDP-CEPH-db Supplement 1	America	Sub	216	G=0.523	A=0.477
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	G=0.93	A=0.07
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.908	A=0.092
Chileans	Chilean	Study-wide	626	G=0.759	A=0.241
Northern Sweden	ACPOP	Study-wide	600	G=0.873	A=0.127
Qatari	Global	Study-wide	216	G=0.801	A=0.199
A Vietnamese Genetic Variation Database	Global	Study-wide	216	G=0.699	A=0.301
SGDP_PRJ	Global	Study-wide	208	G=0.438	A=0.562
The Danish reference pan genome	Danish	Study-wide	40	G=0.95	A=0.05
Siberian	Global	Study-wide	12	G=0.50	A=0.50
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	10	G=1.0	A=0.0

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 10	NC_000010.11:g.12758716G>A
GRCh38.p14 chr 10	NC_000010.11:g.12758716G>C
GRCh38.p14 chr 10	NC_000010.11:g.12758716G>T
GRCh37.p13 chr 10	NC_000010.10:g.12800715G>A
GRCh37.p13 chr 10	NC_000010.10:g.12800715G>C
GRCh37.p13 chr 10	NC_000010.10:g.12800715G>T

Gene: CAMK1D, calcium/calmodulin dependent protein kinase ID (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CAMK1D transcript variant 3	NM_001351032.2:c.9-2232G>A	N/A	Intron Variant
CAMK1D transcript variant 1	NM_020397.4:c.300-2232G>A	N/A	Intron Variant
CAMK1D transcript variant 2	NM_153498.4:c.300-2232G>A	N/A	Intron Variant
CAMK1D transcript variant X2	XM_006717482.4:c.300-2232… XM_006717482.4:c.300-2232G>A	N/A	Intron Variant
CAMK1D transcript variant X3	XM_006717483.5:c.300-2232… XM_006717483.5:c.300-2232G>A	N/A	Intron Variant
CAMK1D transcript variant X1	XM_011519591.4:c.261-2232… XM_011519591.4:c.261-2232G>A	N/A	Intron Variant
CAMK1D transcript variant X4	XM_011519592.4:c.90-2232G… XM_011519592.4:c.90-2232G>A	N/A	Intron Variant
CAMK1D transcript variant X5	XM_011519593.4:c.78-2232G… XM_011519593.4:c.78-2232G>A	N/A	Intron Variant
CAMK1D transcript variant X6	XM_011519595.4:c.9-2232G>A	N/A	Intron Variant
CAMK1D transcript variant X7	XM_047425537.1:c.9-2232G>A	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	G=	A	C	T
GRCh38.p14 chr 10	NC_000010.11:g.12758716=	NC_000010.11:g.12758716G>A	NC_000010.11:g.12758716G>C	NC_000010.11:g.12758716G>T
GRCh37.p13 chr 10	NC_000010.10:g.12800715=	NC_000010.10:g.12800715G>A	NC_000010.10:g.12800715G>C	NC_000010.10:g.12800715G>T
CAMK1D transcript variant 3	NM_001351032.2:c.9-2232=	NM_001351032.2:c.9-2232G>A	NM_001351032.2:c.9-2232G>C	NM_001351032.2:c.9-2232G>T
CAMK1D transcript variant 1	NM_020397.2:c.300-2232=	NM_020397.2:c.300-2232G>A	NM_020397.2:c.300-2232G>C	NM_020397.2:c.300-2232G>T
CAMK1D transcript variant 1	NM_020397.4:c.300-2232=	NM_020397.4:c.300-2232G>A	NM_020397.4:c.300-2232G>C	NM_020397.4:c.300-2232G>T
CAMK1D transcript variant 2	NM_153498.2:c.300-2232=	NM_153498.2:c.300-2232G>A	NM_153498.2:c.300-2232G>C	NM_153498.2:c.300-2232G>T
CAMK1D transcript variant 2	NM_153498.4:c.300-2232=	NM_153498.4:c.300-2232G>A	NM_153498.4:c.300-2232G>C	NM_153498.4:c.300-2232G>T
CAMK1D transcript variant X2	XM_006717482.4:c.300-2232=	XM_006717482.4:c.300-2232G>A	XM_006717482.4:c.300-2232G>C	XM_006717482.4:c.300-2232G>T
CAMK1D transcript variant X3	XM_006717483.5:c.300-2232=	XM_006717483.5:c.300-2232G>A	XM_006717483.5:c.300-2232G>C	XM_006717483.5:c.300-2232G>T
CAMK1D transcript variant X1	XM_011519591.4:c.261-2232=	XM_011519591.4:c.261-2232G>A	XM_011519591.4:c.261-2232G>C	XM_011519591.4:c.261-2232G>T
CAMK1D transcript variant X4	XM_011519592.4:c.90-2232=	XM_011519592.4:c.90-2232G>A	XM_011519592.4:c.90-2232G>C	XM_011519592.4:c.90-2232G>T
CAMK1D transcript variant X5	XM_011519593.4:c.78-2232=	XM_011519593.4:c.78-2232G>A	XM_011519593.4:c.78-2232G>C	XM_011519593.4:c.78-2232G>T
CAMK1D transcript variant X6	XM_011519595.4:c.9-2232=	XM_011519595.4:c.9-2232G>A	XM_011519595.4:c.9-2232G>C	XM_011519595.4:c.9-2232G>T
CAMK1D transcript variant X7	XM_047425537.1:c.9-2232=	XM_047425537.1:c.9-2232G>A	XM_047425537.1:c.9-2232G>C	XM_047425537.1:c.9-2232G>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#.

90 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_SNP	ss15483173	Feb 27, 2004 (120)
2	CSHL-HAPMAP	ss17403317	Feb 27, 2004 (120)
3	SC_SNP	ss18657562	Feb 27, 2004 (120)
4	SC_SNP	ss18896540	Feb 27, 2004 (120)
5	CSHL-HAPMAP	ss19894578	Feb 27, 2004 (120)
6	ABI	ss38510834	Mar 13, 2006 (126)
7	AFFY	ss66393273	Nov 30, 2006 (127)
8	ILLUMINA	ss66666613	Nov 30, 2006 (127)
9	ILLUMINA	ss66898258	Nov 30, 2006 (127)
10	ILLUMINA	ss67010644	Nov 30, 2006 (127)
11	ILLUMINA	ss70377993	May 17, 2007 (127)
12	ILLUMINA	ss70494345	May 24, 2008 (130)
13	ILLUMINA	ss71019315	May 17, 2007 (127)
14	AFFY	ss76135945	Dec 07, 2007 (129)
15	KRIBB_YJKIM	ss84988109	Dec 15, 2007 (130)
16	ILLUMINA	ss107694436	Feb 04, 2009 (130)
17	ILLUMINA	ss121378570	Dec 01, 2009 (131)
18	GMI	ss154601418	Dec 01, 2009 (131)
19	ENSEMBL	ss161309613	Dec 01, 2009 (131)
20	AFFY	ss172607881	Jul 04, 2010 (132)
21	BUSHMAN	ss201163155	Jul 04, 2010 (132)
22	1000GENOMES	ss224574090	Jul 14, 2010 (132)
23	1000GENOMES	ss235061977	Jul 15, 2010 (132)
24	1000GENOMES	ss241791600	Jul 15, 2010 (132)
25	GMI	ss280486882	May 04, 2012 (137)
26	PJP	ss290976967	May 09, 2011 (134)
27	ILLUMINA	ss482509187	May 04, 2012 (137)
28	ILLUMINA	ss484139270	May 04, 2012 (137)
29	ILLUMINA	ss536329114	Sep 08, 2015 (146)
30	TISHKOFF	ss561780262	Apr 25, 2013 (138)
31	SSMP	ss656287446	Apr 25, 2013 (138)
32	ILLUMINA	ss780541507	Sep 08, 2015 (146)
33	ILLUMINA	ss782515255	Sep 08, 2015 (146)
34	ILLUMINA	ss825347604	Apr 01, 2015 (144)
35	ILLUMINA	ss836033346	Sep 08, 2015 (146)
36	EVA-GONL	ss987211674	Aug 21, 2014 (142)
37	JMKIDD_LAB	ss1076773879	Aug 21, 2014 (142)
38	1000GENOMES	ss1336333251	Aug 21, 2014 (142)
39	DDI	ss1426226847	Apr 01, 2015 (144)
40	EVA_GENOME_DK	ss1574928843	Apr 01, 2015 (144)
41	EVA_DECODE	ss1596863628	Apr 01, 2015 (144)
42	EVA_UK10K_ALSPAC	ss1624020575	Apr 01, 2015 (144)
43	EVA_UK10K_TWINSUK	ss1667014608	Apr 01, 2015 (144)
44	EVA_SVP	ss1713158864	Apr 01, 2015 (144)
45	HAMMER_LAB	ss1806262894	Sep 08, 2015 (146)
46	WEILL_CORNELL_DGM	ss1930535796	Feb 12, 2016 (147)
47	GENOMED	ss1967063582	Jul 19, 2016 (147)
48	JJLAB	ss2025992873	Sep 14, 2016 (149)
49	CSHL	ss2136769571	Nov 08, 2017 (151)
50	USC_VALOUEV	ss2154236831	Dec 20, 2016 (150)
51	HUMAN_LONGEVITY	ss2172776990	Dec 20, 2016 (150)
52	SYSTEMSBIOZJU	ss2627465973	Nov 08, 2017 (151)
53	ILLUMINA	ss2632677789	Nov 08, 2017 (151)
54	GRF	ss2698462667	Nov 08, 2017 (151)
55	GNOMAD	ss2885667981	Nov 08, 2017 (151)
56	SWEGEN	ss3005961843	Nov 08, 2017 (151)
57	BIOINF_KMB_FNS_UNIBA	ss3026781632	Nov 08, 2017 (151)
58	CSHL	ss3348969567	Nov 08, 2017 (151)
59	ILLUMINA	ss3626390826	Oct 12, 2018 (152)
60	ILLUMINA	ss3630705315	Oct 12, 2018 (152)
61	ILLUMINA	ss3638933120	Oct 12, 2018 (152)
62	ILLUMINA	ss3639466032	Oct 12, 2018 (152)
63	ILLUMINA	ss3641663205	Oct 12, 2018 (152)
64	EGCUT_WGS	ss3673490958	Jul 13, 2019 (153)
65	EVA_DECODE	ss3689311984	Jul 13, 2019 (153)
66	ACPOP	ss3737075747	Jul 13, 2019 (153)
67	EVA	ss3747765160	Jul 13, 2019 (153)
68	KHV_HUMAN_GENOMES	ss3813126194	Jul 13, 2019 (153)
69	EVA	ss3831976674	Apr 26, 2020 (154)
70	EVA	ss3839519889	Apr 26, 2020 (154)
71	EVA	ss3844986340	Apr 26, 2020 (154)
72	HGDP	ss3847376338	Apr 26, 2020 (154)
73	SGDP_PRJ	ss3873565903	Apr 26, 2020 (154)
74	KRGDB	ss3921512025	Apr 26, 2020 (154)
75	EVA	ss3985459120	Apr 26, 2021 (155)
76	TOPMED	ss4842917908	Apr 26, 2021 (155)
77	TOMMO_GENOMICS	ss5196330573	Apr 26, 2021 (155)
78	1000G_HIGH_COVERAGE	ss5282971247	Oct 16, 2022 (156)
79	EVA	ss5315453031	Oct 16, 2022 (156)
80	EVA	ss5391686288	Oct 16, 2022 (156)
81	HUGCELL_USP	ss5478743635	Oct 16, 2022 (156)
82	1000G_HIGH_COVERAGE	ss5576381288	Oct 16, 2022 (156)
83	SANFORD_IMAGENETICS	ss5648705574	Oct 16, 2022 (156)
84	TOMMO_GENOMICS	ss5741198500	Oct 16, 2022 (156)
85	YY_MCH	ss5811209168	Oct 16, 2022 (156)
86	EVA	ss5823997957	Oct 16, 2022 (156)
87	EVA	ss5849444248	Oct 16, 2022 (156)
88	EVA	ss5877794943	Oct 16, 2022 (156)
89	EVA	ss5939991632	Oct 16, 2022 (156)
90	EVA	ss5980596256	Oct 16, 2022 (156)
91	1000Genomes	NC_000010.10 - 12800715	Oct 12, 2018 (152)
92	1000Genomes_30x	NC_000010.11 - 12758716	Oct 16, 2022 (156)
93	The Avon Longitudinal Study of Parents and Children	NC_000010.10 - 12800715	Oct 12, 2018 (152)
94	Chileans	NC_000010.10 - 12800715	Apr 26, 2020 (154)
95	Genetic variation in the Estonian population	NC_000010.10 - 12800715	Oct 12, 2018 (152)
96	The Danish reference pan genome	NC_000010.10 - 12800715	Apr 26, 2020 (154)
97	gnomAD - Genomes	NC_000010.11 - 12758716	Apr 26, 2021 (155)
98	Genome of the Netherlands Release 5	NC_000010.10 - 12800715	Apr 26, 2020 (154)
99	HGDP-CEPH-db Supplement 1	NC_000010.9 - 12840721	Apr 26, 2020 (154)
100	KOREAN population from KRGDB	NC_000010.10 - 12800715	Apr 26, 2020 (154)
101	Northern Sweden	NC_000010.10 - 12800715	Jul 13, 2019 (153)
102	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000010.10 - 12800715	Apr 26, 2021 (155)
103	Qatari	NC_000010.10 - 12800715	Apr 26, 2020 (154)
104	SGDP_PRJ	NC_000010.10 - 12800715	Apr 26, 2020 (154)
105	Siberian	NC_000010.10 - 12800715	Apr 26, 2020 (154)
106	8.3KJPN	NC_000010.10 - 12800715	Apr 26, 2021 (155)
107	14KJPN	NC_000010.11 - 12758716	Oct 16, 2022 (156)
108	TopMed	NC_000010.11 - 12758716	Apr 26, 2021 (155)
109	UK 10K study - Twins	NC_000010.10 - 12800715	Oct 12, 2018 (152)
110	A Vietnamese Genetic Variation Database	NC_000010.10 - 12800715	Jul 13, 2019 (153)
111	ALFA	NC_000010.11 - 12758716	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)
rs58182288	May 24, 2008 (130)
rs117950370	Aug 16, 2010 (132)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3638933120, ss3639466032	NC_000010.8:12840720:G:A	NC_000010.11:12758715:G:A	(self)
54230, ss66393273, ss76135945, ss172607881, ss201163155, ss280486882, ss290976967, ss482509187, ss825347604, ss1596863628, ss1713158864, ss2136769571, ss3847376338	NC_000010.9:12840720:G:A	NC_000010.11:12758715:G:A	(self)
48681881, 27052276, 42851, 19229206, 2038569, 12064887, 28689419, 10360612, 685047, 12577726, 25582883, 6753185, 54299880, 27052276, 6005633, ss224574090, ss235061977, ss241791600, ss484139270, ss536329114, ss561780262, ss656287446, ss780541507, ss782515255, ss836033346, ss987211674, ss1076773879, ss1336333251, ss1426226847, ss1574928843, ss1624020575, ss1667014608, ss1806262894, ss1930535796, ss1967063582, ss2025992873, ss2154236831, ss2627465973, ss2632677789, ss2698462667, ss2885667981, ss3005961843, ss3348969567, ss3626390826, ss3630705315, ss3641663205, ss3673490958, ss3737075747, ss3747765160, ss3831976674, ss3839519889, ss3873565903, ss3921512025, ss3985459120, ss5196330573, ss5315453031, ss5391686288, ss5648705574, ss5823997957, ss5939991632, ss5980596256	NC_000010.10:12800714:G:A	NC_000010.11:12758715:G:A	(self)
63907223, 343850380, 75035604, 58463563, 10782648503, ss2172776990, ss3026781632, ss3689311984, ss3813126194, ss3844986340, ss4842917908, ss5282971247, ss5478743635, ss5576381288, ss5741198500, ss5811209168, ss5849444248, ss5877794943	NC_000010.11:12758715:G:A	NC_000010.11:12758715:G:A	(self)
ss38510834, ss66666613, ss66898258, ss67010644, ss70377993, ss70494345, ss71019315, ss84988109, ss107694436, ss121378570, ss154601418, ss161309613	NT_008705.16:12740714:G:A	NC_000010.11:12758715:G:A	(self)
ss15483173, ss17403317, ss18657562, ss18896540, ss19894578	NT_077569.2:7163610:G:A	NC_000010.11:12758715:G:A	(self)
28689419, ss3921512025	NC_000010.10:12800714:G:C	NC_000010.11:12758715:G:C	(self)
ss38510834, ss70377993, ss71019315	NT_008705.16:12740714:G:T	NC_000010.11:12758715:G: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 rs10752275

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

rs10752275