Name: rs10925290
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.

rs10925290

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:237010955 (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: T=0.098942 (26189/264690, TOPMED)
A=0.040619 (4981/122628, ALFA)
T=0.1084 (694/6404, 1000G_30x) (+ 12 more)
T=0.1052 (527/5008, 1000G)
T=0.0429 (192/4480, Estonian)
A=0.3113 (912/2930, KOREAN)
A=0.2280 (363/1592, HapMap)
A=0.0685 (77/1124, Daghestan)
T=0.033 (33/998, GoNL)
T=0.070 (42/600, NorthernSweden)
A=0.014 (3/212, Qatari)
A=0.330 (60/182, SGDP_PRJ)
T=0.03 (1/40, GENOME_DK)
C=0.5 (4/8, Siberian)
T=0.5 (4/8, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
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	122628	C=0.957824	A=0.040619, T=0.001558
European	Sub	111298	C=0.963701	A=0.034592, T=0.001707
African	Sub	4728	C=0.8589	A=0.1411, T=0.0000
African Others	Sub	180	C=0.806	A=0.194, T=0.000
African American	Sub	4548	C=0.8610	A=0.1390, T=0.0000
Asian	Sub	262	C=0.740	A=0.260, T=0.000
East Asian	Sub	176	C=0.693	A=0.307, T=0.000
Other Asian	Sub	86	C=0.84	A=0.16, T=0.00
Latin American 1	Sub	620	C=0.932	A=0.068, T=0.000
Latin American 2	Sub	1954	C=0.9611	A=0.0389, T=0.0000
South Asian	Sub	132	C=0.955	A=0.045, T=0.000
Other	Sub	3634	C=0.9249	A=0.0748, T=0.0003

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	C=0.901058	T=0.098942
Allele Frequency Aggregator	Total	Global	122628	C=0.957824	A=0.040619, T=0.001558
Allele Frequency Aggregator	European	Sub	111298	C=0.963701	A=0.034592, T=0.001707
Allele Frequency Aggregator	African	Sub	4728	C=0.8589	A=0.1411, T=0.0000
Allele Frequency Aggregator	Other	Sub	3634	C=0.9249	A=0.0748, T=0.0003
Allele Frequency Aggregator	Latin American 2	Sub	1954	C=0.9611	A=0.0389, T=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	620	C=0.932	A=0.068, T=0.000
Allele Frequency Aggregator	Asian	Sub	262	C=0.740	A=0.260, T=0.000
Allele Frequency Aggregator	South Asian	Sub	132	C=0.955	A=0.045, T=0.000
1000Genomes_30x	Global	Study-wide	6404	C=0.8118	A=0.0798, T=0.1084
1000Genomes_30x	African	Sub	1786	C=0.7284	A=0.0000, T=0.2716
1000Genomes_30x	Europe	Sub	1266	C=0.9621	A=0.0000, T=0.0379
1000Genomes_30x	South Asian	Sub	1202	C=0.8569	A=0.0782, T=0.0649
1000Genomes_30x	East Asian	Sub	1170	C=0.6624	A=0.3009, T=0.0368
1000Genomes_30x	American	Sub	980	C=0.893	A=0.066, T=0.041
1000Genomes	Global	Study-wide	5008	C=0.8093	A=0.0855, T=0.1052
1000Genomes	African	Sub	1322	C=0.7277	A=0.0015, T=0.2708
1000Genomes	East Asian	Sub	1008	C=0.6607	A=0.3026, T=0.0367
1000Genomes	Europe	Sub	1006	C=0.9652	A=0.0000, T=0.0348
1000Genomes	South Asian	Sub	978	C=0.850	A=0.080, T=0.071
1000Genomes	American	Sub	694	C=0.898	A=0.062, T=0.040
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.9571	T=0.0429
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.6379	A=0.3113, G=0.0000, T=0.0509
HapMap	Global	Study-wide	1592	C=0.7720	A=0.2280
HapMap	American	Sub	766	C=0.825	A=0.175
HapMap	African	Sub	400	C=0.688	A=0.312
HapMap	Asian	Sub	254	C=0.606	A=0.394
HapMap	Europe	Sub	172	C=0.977	A=0.023
Genome-wide autozygosity in Daghestan	Global	Study-wide	1124	C=0.9315	A=0.0685
Genome-wide autozygosity in Daghestan	Daghestan	Sub	620	C=0.950	A=0.050
Genome-wide autozygosity in Daghestan	Near_East	Sub	140	C=0.879	A=0.121
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	C=0.893	A=0.107
Genome-wide autozygosity in Daghestan	Europe	Sub	108	C=0.954	A=0.046
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	C=0.90	A=0.10
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	C=0.97	A=0.03
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.967	T=0.033
Northern Sweden	ACPOP	Study-wide	600	C=0.930	T=0.070
Qatari	Global	Study-wide	212	C=0.986	A=0.014
SGDP_PRJ	Global	Study-wide	182	C=0.385	A=0.330, T=0.286
The Danish reference pan genome	Danish	Study-wide	40	C=0.97	T=0.03
Siberian	Global	Study-wide	8	C=0.5	T=0.5

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 1	NC_000001.11:g.237010955C>A
GRCh38.p14 chr 1	NC_000001.11:g.237010955C>G
GRCh38.p14 chr 1	NC_000001.11:g.237010955C>T
GRCh37.p13 chr 1	NC_000001.10:g.237174255C>A
GRCh37.p13 chr 1	NC_000001.10:g.237174255C>G
GRCh37.p13 chr 1	NC_000001.10:g.237174255C>T

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 1	NC_000001.11:g.237010955=	NC_000001.11:g.237010955C>A	NC_000001.11:g.237010955C>G	NC_000001.11:g.237010955C>T
GRCh37.p13 chr 1	NC_000001.10:g.237174255=	NC_000001.10:g.237174255C>A	NC_000001.10:g.237174255C>G	NC_000001.10:g.237174255C>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#.

92 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_SNP	ss18069706	Feb 27, 2004 (120)
2	CSHL-HAPMAP	ss19829354	Feb 27, 2004 (120)
3	ABI	ss41146457	Mar 13, 2006 (126)
4	ILLUMINA	ss75089362	Dec 06, 2007 (129)
5	1000GENOMES	ss111988383	Jan 25, 2009 (130)
6	KRIBB_YJKIM	ss119651593	Dec 01, 2009 (131)
7	GMI	ss156461624	Dec 01, 2009 (131)
8	ILLUMINA	ss159939157	Dec 01, 2009 (131)
9	ENSEMBL	ss161232636	Dec 01, 2009 (131)
10	COMPLETE_GENOMICS	ss165475885	Jul 04, 2010 (132)
11	COMPLETE_GENOMICS	ss167573296	Jul 04, 2010 (132)
12	ILLUMINA	ss170759959	Jul 04, 2010 (132)
13	BUSHMAN	ss199795296	Jul 04, 2010 (132)
14	1000GENOMES	ss218960243	Jul 14, 2010 (132)
15	1000GENOMES	ss230961148	Jul 14, 2010 (132)
16	1000GENOMES	ss238563961	Jul 15, 2010 (132)
17	GMI	ss276276007	May 04, 2012 (137)
18	ILLUMINA	ss479405813	May 04, 2012 (137)
19	ILLUMINA	ss479409162	May 04, 2012 (137)
20	ILLUMINA	ss479822707	Sep 08, 2015 (146)
21	ILLUMINA	ss484502851	May 04, 2012 (137)
22	ILLUMINA	ss536653871	Sep 08, 2015 (146)
23	TISHKOFF	ss555232093	Apr 25, 2013 (138)
24	ILLUMINA	ss778370828	Sep 08, 2015 (146)
25	ILLUMINA	ss782697984	Sep 08, 2015 (146)
26	ILLUMINA	ss783666071	Sep 08, 2015 (146)
27	ILLUMINA	ss831949081	Sep 08, 2015 (146)
28	ILLUMINA	ss833825700	Sep 08, 2015 (146)
29	EVA-GONL	ss976297131	Aug 21, 2014 (142)
30	JMKIDD_LAB	ss1068716844	Aug 21, 2014 (142)
31	1000GENOMES	ss1295217937	Aug 21, 2014 (142)
32	1000GENOMES	ss1295217938	Aug 21, 2014 (142)
33	HAMMER_LAB	ss1397276903	Sep 08, 2015 (146)
34	DDI	ss1426156124	Apr 01, 2015 (144)
35	EVA_GENOME_DK	ss1574777429	Apr 01, 2015 (144)
36	EVA_DECODE	ss1585699028	Apr 01, 2015 (144)
37	EVA_DECODE	ss1585699029	Apr 01, 2015 (144)
38	EVA_UK10K_ALSPAC	ss1602444645	Apr 01, 2015 (144)
39	EVA_UK10K_ALSPAC	ss1602444646	Apr 01, 2015 (144)
40	EVA_UK10K_TWINSUK	ss1645438678	Apr 01, 2015 (144)
41	EVA_UK10K_TWINSUK	ss1645438679	Apr 01, 2015 (144)
42	EVA_SVP	ss1712417118	Apr 01, 2015 (144)
43	ILLUMINA	ss1751907340	Sep 08, 2015 (146)
44	HAMMER_LAB	ss1795946712	Sep 08, 2015 (146)
45	WEILL_CORNELL_DGM	ss1919518554	Feb 12, 2016 (147)
46	GENOMED	ss1967009256	Jul 19, 2016 (147)
47	USC_VALOUEV	ss2148323098	Nov 08, 2017 (151)
48	HUMAN_LONGEVITY	ss2171255305	Dec 20, 2016 (150)
49	SYSTEMSBIOZJU	ss2624656048	Nov 08, 2017 (151)
50	ILLUMINA	ss2632648468	Nov 08, 2017 (151)
51	GRF	ss2698325717	Nov 08, 2017 (151)
52	GNOMAD	ss2767818103	Nov 08, 2017 (151)
53	SWEGEN	ss2988686804	Nov 08, 2017 (151)
54	SWEGEN	ss2988686805	Nov 08, 2017 (151)
55	ILLUMINA	ss3626342818	Oct 11, 2018 (152)
56	ILLUMINA	ss3630677369	Oct 11, 2018 (152)
57	ILLUMINA	ss3632931009	Oct 11, 2018 (152)
58	ILLUMINA	ss3633627327	Oct 11, 2018 (152)
59	ILLUMINA	ss3634380780	Oct 11, 2018 (152)
60	ILLUMINA	ss3635320300	Oct 11, 2018 (152)
61	ILLUMINA	ss3636059736	Oct 11, 2018 (152)
62	ILLUMINA	ss3637070856	Oct 11, 2018 (152)
63	ILLUMINA	ss3637822877	Oct 11, 2018 (152)
64	ILLUMINA	ss3640088133	Oct 11, 2018 (152)
65	ILLUMINA	ss3642828465	Oct 11, 2018 (152)
66	EGCUT_WGS	ss3656645704	Jul 12, 2019 (153)
67	EVA_DECODE	ss3688913250	Jul 12, 2019 (153)
68	EVA_DECODE	ss3688913251	Jul 12, 2019 (153)
69	ACPOP	ss3727989011	Jul 12, 2019 (153)
70	ILLUMINA	ss3744681687	Jul 12, 2019 (153)
71	EVA	ss3747515717	Jul 12, 2019 (153)
72	ILLUMINA	ss3772182461	Jul 12, 2019 (153)
73	KHV_HUMAN_GENOMES	ss3800518068	Jul 12, 2019 (153)
74	KHV_HUMAN_GENOMES	ss3800518069	Jul 12, 2019 (153)
75	SGDP_PRJ	ss3851196391	Apr 25, 2020 (154)
76	KRGDB	ss3896553290	Apr 25, 2020 (154)
77	TOPMED	ss4488500617	Apr 25, 2021 (155)
78	TOMMO_GENOMICS	ss5149085123	Apr 25, 2021 (155)
79	TOMMO_GENOMICS	ss5149085124	Apr 25, 2021 (155)
80	1000G_HIGH_COVERAGE	ss5246294069	Oct 17, 2022 (156)
81	EVA	ss5314694358	Oct 17, 2022 (156)
82	HUGCELL_USP	ss5446681785	Oct 17, 2022 (156)
83	HUGCELL_USP	ss5446681786	Oct 17, 2022 (156)
84	1000G_HIGH_COVERAGE	ss5520635500	Oct 17, 2022 (156)
85	SANFORD_IMAGENETICS	ss5627730180	Oct 17, 2022 (156)
86	TOMMO_GENOMICS	ss5677036145	Oct 17, 2022 (156)
87	TOMMO_GENOMICS	ss5677036146	Oct 17, 2022 (156)
88	YY_MCH	ss5801767606	Oct 17, 2022 (156)
89	EVA	ss5833464973	Oct 17, 2022 (156)
90	EVA	ss5833464974	Oct 17, 2022 (156)
91	EVA	ss5849351075	Oct 17, 2022 (156)
92	EVA	ss5939581420	Oct 17, 2022 (156)
93	1000Genomes	NC_000001.10 - 237174255	Oct 11, 2018 (152)
94	1000Genomes_30x	NC_000001.11 - 237010955	Oct 17, 2022 (156)
95	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 3374376 (NC_000001.10:237174254:C:C 3726/3854, NC_000001.10:237174254:C:T 128/3854) Row 3374377 (NC_000001.10:237174254:C:C 3847/3854, NC_000001.10:237174254:C:A 7/3854)	-	Oct 11, 2018 (152)
96	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 3374376 (NC_000001.10:237174254:C:C 3726/3854, NC_000001.10:237174254:C:T 128/3854) Row 3374377 (NC_000001.10:237174254:C:C 3847/3854, NC_000001.10:237174254:C:A 7/3854)	-	Oct 11, 2018 (152)
97	Genome-wide autozygosity in Daghestan	NC_000001.9 - 235240878	Apr 25, 2020 (154)
98	Genetic variation in the Estonian population	NC_000001.10 - 237174255	Oct 11, 2018 (152)
99	The Danish reference pan genome	NC_000001.10 - 237174255	Apr 25, 2020 (154)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 43652368 (NC_000001.11:237010954:C:A 1691/140124) Row 43652369 (NC_000001.11:237010954:C:T 13396/140104)	-	Apr 25, 2021 (155)
101	gnomAD - Genomes Submission ignored due to conflicting rows: Row 43652368 (NC_000001.11:237010954:C:A 1691/140124) Row 43652369 (NC_000001.11:237010954:C:T 13396/140104)	-	Apr 25, 2021 (155)
102	Genome of the Netherlands Release 5	NC_000001.10 - 237174255	Apr 25, 2020 (154)
103	HapMap	NC_000001.11 - 237010955	Apr 25, 2020 (154)
104	KOREAN population from KRGDB	NC_000001.10 - 237174255	Apr 25, 2020 (154)
105	Northern Sweden	NC_000001.10 - 237174255	Jul 12, 2019 (153)
106	Qatari	NC_000001.10 - 237174255	Apr 25, 2020 (154)
107	SGDP_PRJ	NC_000001.10 - 237174255	Apr 25, 2020 (154)
108	Siberian	NC_000001.10 - 237174255	Apr 25, 2020 (154)
109	8.3KJPN Submission ignored due to conflicting rows: Row 7054430 (NC_000001.10:237174254:C:A 6227/16760) Row 7054431 (NC_000001.10:237174254:C:T 711/16760)	-	Apr 25, 2021 (155)
110	8.3KJPN Submission ignored due to conflicting rows: Row 7054430 (NC_000001.10:237174254:C:A 6227/16760) Row 7054431 (NC_000001.10:237174254:C:T 711/16760)	-	Apr 25, 2021 (155)
111	14KJPN Submission ignored due to conflicting rows: Row 10873249 (NC_000001.11:237010954:C:A 10455/28256) Row 10873250 (NC_000001.11:237010954:C:T 1195/28256)	-	Oct 17, 2022 (156)
112	14KJPN Submission ignored due to conflicting rows: Row 10873249 (NC_000001.11:237010954:C:A 10455/28256) Row 10873250 (NC_000001.11:237010954:C:T 1195/28256)	-	Oct 17, 2022 (156)
113	TopMed	NC_000001.11 - 237010955	Apr 25, 2021 (155)
114	UK 10K study - Twins Submission ignored due to conflicting rows: Row 3374376 (NC_000001.10:237174254:C:C 3579/3708, NC_000001.10:237174254:C:T 129/3708) Row 3374377 (NC_000001.10:237174254:C:C 3704/3708, NC_000001.10:237174254:C:A 4/3708)	-	Oct 11, 2018 (152)
115	UK 10K study - Twins Submission ignored due to conflicting rows: Row 3374376 (NC_000001.10:237174254:C:C 3579/3708, NC_000001.10:237174254:C:T 129/3708) Row 3374377 (NC_000001.10:237174254:C:C 3704/3708, NC_000001.10:237174254:C:A 4/3708)	-	Oct 11, 2018 (152)
116	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 734432 (NC_000001.10:237174254:C:C 154/163, NC_000001.10:237174254:C:T 9/163) Row 734433 (NC_000001.10:237174254:C:C 154/207, NC_000001.10:237174254:C:A 53/207)	-	Jul 12, 2019 (153)
117	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 734432 (NC_000001.10:237174254:C:C 154/163, NC_000001.10:237174254:C:T 9/163) Row 734433 (NC_000001.10:237174254:C:C 154/207, NC_000001.10:237174254:C:A 53/207)	-	Jul 12, 2019 (153)
118	ALFA	NC_000001.11 - 237010955	Apr 25, 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)
rs117019876	Aug 16, 2010 (132)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
37989, ss276276007, ss479405813, ss1397276903, ss1585699028, ss1712417118, ss3642828465	NC_000001.9:235240877:C:A	NC_000001.11:237010954:C:A	(self)
6093468, 3730684, 1560484, 3213371, ss218960243, ss230961148, ss238563961, ss479409162, ss479822707, ss484502851, ss536653871, ss778370828, ss782697984, ss783666071, ss831949081, ss833825700, ss1068716844, ss1295217937, ss1602444646, ss1645438679, ss1751907340, ss1919518554, ss2632648468, ss2698325717, ss2767818103, ss2988686805, ss3626342818, ss3630677369, ss3632931009, ss3633627327, ss3634380780, ss3635320300, ss3636059736, ss3637070856, ss3637822877, ss3640088133, ss3744681687, ss3747515717, ss3772182461, ss3851196391, ss3896553290, ss5149085123, ss5314694358, ss5627730180, ss5833464974, ss5939581420	NC_000001.10:237174254:C:A	NC_000001.11:237010954:C:A	(self)
8161435, 298442, 6024230634, ss2171255305, ss3688913250, ss3800518069, ss5446681786, ss5520635500, ss5677036145, ss5801767606, ss5849351075	NC_000001.11:237010954:C:A	NC_000001.11:237010954:C:A	(self)
ss18069706, ss19829354	NT_004836.15:1932043:C:A	NC_000001.11:237010954:C:A	(self)
ss41146457, ss75089362, ss119651593, ss159939157, ss161232636, ss170759959	NT_167186.1:30692033:C:A	NC_000001.11:237010954:C:A	(self)
3730684, ss3896553290	NC_000001.10:237174254:C:G	NC_000001.11:237010954:C:G	(self)
ss111988383, ss165475885, ss167573296, ss199795296, ss276276007, ss1585699029	NC_000001.9:235240877:C:T	NC_000001.11:237010954:C:T	(self)
6093468, 2383952, 1946280, 1476132, 3730684, 1273876, 3213371, 839452, ss218960243, ss230961148, ss238563961, ss555232093, ss976297131, ss1295217938, ss1426156124, ss1574777429, ss1602444645, ss1645438678, ss1795946712, ss1967009256, ss2148323098, ss2624656048, ss2767818103, ss2988686804, ss3656645704, ss3727989011, ss3851196391, ss3896553290, ss5149085124, ss5627730180, ss5833464973	NC_000001.10:237174254:C:T	NC_000001.11:237010954:C:T	(self)
8161435, 52106952, 6024230634, ss2171255305, ss3688913251, ss3800518068, ss4488500617, ss5246294069, ss5446681785, ss5520635500, ss5677036146, ss5801767606, ss5849351075	NC_000001.11:237010954:C:T	NC_000001.11:237010954:C:T	(self)
ss156461624	NT_167186.1:30692033:C:T	NC_000001.11:237010954: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 rs10925290

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

rs10925290