Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

dbSNP Short Genetic Variations

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.

rs10925924

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr1:239603845 (GRCh38.p13) 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
T>A / T>C / T>G
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.368318 (97490/264690, TOPMED)
T=0.353712 (49502/139950, GnomAD)
T=0.27805 (6274/22564, ALFA) (+ 15 more)
T=0.18461 (3094/16760, 8.3KJPN)
T=0.3930 (1968/5008, 1000G)
T=0.1600 (717/4480, Estonian)
T=0.1772 (683/3854, ALSPAC)
T=0.1491 (553/3708, TWINSUK)
T=0.2068 (606/2930, KOREAN)
T=0.2003 (367/1832, Korea1K)
G=0.4700 (501/1066, HapMap)
T=0.163 (163/998, GoNL)
T=0.187 (112/600, NorthernSweden)
T=0.143 (68/474, SGDP_PRJ)
T=0.264 (57/216, Qatari)
T=0.124 (26/210, Vietnamese)
T=0.21 (11/52, Siberian)
T=0.15 (6/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
CHRM3 : Intron Variant
LOC105373225 : Intron Variant
Publications
0 citations
Genomic View
See rs on genome
Help

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.p13 chr 1 NC_000001.11:g.239603845T>A
GRCh38.p13 chr 1 NC_000001.11:g.239603845T>C
GRCh38.p13 chr 1 NC_000001.11:g.239603845T>G
GRCh37.p13 chr 1 NC_000001.10:g.239767145T>A
GRCh37.p13 chr 1 NC_000001.10:g.239767145T>C
GRCh37.p13 chr 1 NC_000001.10:g.239767145T>G
CHRM3 RefSeqGene NG_032046.2:g.221916T>A
CHRM3 RefSeqGene NG_032046.2:g.221916T>C
CHRM3 RefSeqGene NG_032046.2:g.221916T>G
Gene: CHRM3, cholinergic receptor muscarinic 3 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
CHRM3 transcript variant 1 NM_001347716.2:c.-541-283…

NM_001347716.2:c.-541-28379T>A

N/A Intron Variant
CHRM3 transcript variant 3 NM_001375978.1:c.-312-283…

NM_001375978.1:c.-312-28379T>A

N/A Intron Variant
CHRM3 transcript variant 4 NM_001375979.1:c.-250+580…

NM_001375979.1:c.-250+58096T>A

N/A Intron Variant
CHRM3 transcript variant 5 NM_001375980.1:c.-250+580…

NM_001375980.1:c.-250+58096T>A

N/A Intron Variant
CHRM3 transcript variant 6 NM_001375981.1:c.-312-283…

NM_001375981.1:c.-312-28379T>A

N/A Intron Variant
CHRM3 transcript variant 7 NM_001375982.1:c.-312-283…

NM_001375982.1:c.-312-28379T>A

N/A Intron Variant
CHRM3 transcript variant 8 NM_001375983.1:c.-354+580…

NM_001375983.1:c.-354+58096T>A

N/A Intron Variant
CHRM3 transcript variant 9 NM_001375984.1:c.-416-283…

NM_001375984.1:c.-416-28379T>A

N/A Intron Variant
CHRM3 transcript variant 10 NM_001375985.1:c.-354+580…

NM_001375985.1:c.-354+58096T>A

N/A Intron Variant
CHRM3 transcript variant 2 NM_000740.4:c. N/A Genic Upstream Transcript Variant
CHRM3 transcript variant 11 NR_164748.1:n. N/A Intron Variant
CHRM3 transcript variant X4 XM_011544043.2:c.-645-283…

XM_011544043.2:c.-645-28379T>A

N/A Intron Variant
CHRM3 transcript variant X5 XM_011544044.2:c.-416-283…

XM_011544044.2:c.-416-28379T>A

N/A Intron Variant
CHRM3 transcript variant X10 XM_011544047.2:c.-185-283…

XM_011544047.2:c.-185-28379T>A

N/A Intron Variant
CHRM3 transcript variant X2 XM_017000152.2:c.-312-283…

XM_017000152.2:c.-312-28379T>A

N/A Intron Variant
CHRM3 transcript variant X9 XM_017000154.1:c.-312-283…

XM_017000154.1:c.-312-28379T>A

N/A Intron Variant
CHRM3 transcript variant X12 XM_017000157.2:c.-313+136…

XM_017000157.2:c.-313+13640T>A

N/A Intron Variant
CHRM3 transcript variant X14 XM_017000159.1:c.-123+580…

XM_017000159.1:c.-123+58096T>A

N/A Intron Variant
CHRM3 transcript variant X17 XM_017000162.1:c.-185-283…

XM_017000162.1:c.-185-28379T>A

N/A Intron Variant
CHRM3 transcript variant X15 XM_017000160.2:c. N/A Genic Upstream Transcript Variant
CHRM3 transcript variant X18 XM_017000163.2:c. N/A Genic Upstream Transcript Variant
Gene: LOC105373225, uncharacterized LOC105373225 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
LOC105373225 transcript variant X1 XR_001738554.1:n. N/A Intron Variant
LOC105373225 transcript variant X2 XR_001738555.1:n. N/A Intron Variant
LOC105373225 transcript variant X3 XR_001738556.1:n. N/A Intron Variant
LOC105373225 transcript variant X4 XR_001738557.1:n. N/A Intron Variant
LOC105373225 transcript variant X5 XR_001738558.1:n. N/A Intron Variant
Help

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

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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 22564 T=0.27805 G=0.72195
European Sub 15646 T=0.16145 G=0.83855
African Sub 3620 T=0.7989 G=0.2011
African Others Sub 126 T=0.944 G=0.056
African American Sub 3494 T=0.7936 G=0.2064
Asian Sub 160 T=0.175 G=0.825
East Asian Sub 102 T=0.245 G=0.755
Other Asian Sub 58 T=0.05 G=0.95
Latin American 1 Sub 250 T=0.288 G=0.712
Latin American 2 Sub 1590 T=0.2258 G=0.7742
South Asian Sub 110 T=0.309 G=0.691
Other Sub 1188 T=0.3056 G=0.6944


Help

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 T=0.368318 G=0.631682
gnomAD - Genomes Global Study-wide 139950 T=0.353712 G=0.646288
gnomAD - Genomes European Sub 75830 T=0.15754 G=0.84246
gnomAD - Genomes African Sub 41906 T=0.78347 G=0.21653
gnomAD - Genomes American Sub 13618 T=0.23205 G=0.76795
gnomAD - Genomes Ashkenazi Jewish Sub 3322 T=0.1325 G=0.8675
gnomAD - Genomes East Asian Sub 3124 T=0.1559 G=0.8441
gnomAD - Genomes Other Sub 2150 T=0.2963 G=0.7037
8.3KJPN JAPANESE Study-wide 16760 T=0.18461 G=0.81539
1000Genomes Global Study-wide 5008 T=0.3930 G=0.6070
1000Genomes African Sub 1322 T=0.9115 G=0.0885
1000Genomes East Asian Sub 1008 T=0.1716 G=0.8284
1000Genomes Europe Sub 1006 T=0.1630 G=0.8370
1000Genomes South Asian Sub 978 T=0.270 G=0.730
1000Genomes American Sub 694 T=0.233 G=0.767
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.1600 G=0.8400
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.1772 G=0.8228
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.1491 G=0.8509
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.2068 A=0.0000, C=0.0000, G=0.7932
Korean Genome Project KOREAN Study-wide 1832 T=0.2003 G=0.7997
HapMap Global Study-wide 1066 T=0.5300 G=0.4700
HapMap African Sub 512 T=0.801 G=0.199
HapMap American Sub 306 T=0.330 G=0.670
HapMap Asian Sub 248 T=0.218 G=0.782
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.163 G=0.837
Northern Sweden ACPOP Study-wide 600 T=0.187 G=0.813
SGDP_PRJ Global Study-wide 474 T=0.143 G=0.857
Qatari Global Study-wide 216 T=0.264 G=0.736
A Vietnamese Genetic Variation Database Global Study-wide 210 T=0.124 G=0.876
Siberian Global Study-wide 52 T=0.21 G=0.79
The Danish reference pan genome Danish Study-wide 40 T=0.15 G=0.85
Help

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 T= A C G
GRCh38.p13 chr 1 NC_000001.11:g.239603845= NC_000001.11:g.239603845T>A NC_000001.11:g.239603845T>C NC_000001.11:g.239603845T>G
GRCh37.p13 chr 1 NC_000001.10:g.239767145= NC_000001.10:g.239767145T>A NC_000001.10:g.239767145T>C NC_000001.10:g.239767145T>G
CHRM3 RefSeqGene NG_032046.2:g.221916= NG_032046.2:g.221916T>A NG_032046.2:g.221916T>C NG_032046.2:g.221916T>G
CHRM3 transcript variant 1 NM_001347716.2:c.-541-28379= NM_001347716.2:c.-541-28379T>A NM_001347716.2:c.-541-28379T>C NM_001347716.2:c.-541-28379T>G
CHRM3 transcript variant 3 NM_001375978.1:c.-312-28379= NM_001375978.1:c.-312-28379T>A NM_001375978.1:c.-312-28379T>C NM_001375978.1:c.-312-28379T>G
CHRM3 transcript variant 4 NM_001375979.1:c.-250+58096= NM_001375979.1:c.-250+58096T>A NM_001375979.1:c.-250+58096T>C NM_001375979.1:c.-250+58096T>G
CHRM3 transcript variant 5 NM_001375980.1:c.-250+58096= NM_001375980.1:c.-250+58096T>A NM_001375980.1:c.-250+58096T>C NM_001375980.1:c.-250+58096T>G
CHRM3 transcript variant 6 NM_001375981.1:c.-312-28379= NM_001375981.1:c.-312-28379T>A NM_001375981.1:c.-312-28379T>C NM_001375981.1:c.-312-28379T>G
CHRM3 transcript variant 7 NM_001375982.1:c.-312-28379= NM_001375982.1:c.-312-28379T>A NM_001375982.1:c.-312-28379T>C NM_001375982.1:c.-312-28379T>G
CHRM3 transcript variant 8 NM_001375983.1:c.-354+58096= NM_001375983.1:c.-354+58096T>A NM_001375983.1:c.-354+58096T>C NM_001375983.1:c.-354+58096T>G
CHRM3 transcript variant 9 NM_001375984.1:c.-416-28379= NM_001375984.1:c.-416-28379T>A NM_001375984.1:c.-416-28379T>C NM_001375984.1:c.-416-28379T>G
CHRM3 transcript variant 10 NM_001375985.1:c.-354+58096= NM_001375985.1:c.-354+58096T>A NM_001375985.1:c.-354+58096T>C NM_001375985.1:c.-354+58096T>G
CHRM3 transcript variant X1 XM_005273031.1:c.-312-28379= XM_005273031.1:c.-312-28379T>A XM_005273031.1:c.-312-28379T>C XM_005273031.1:c.-312-28379T>G
CHRM3 transcript variant X2 XM_005273032.1:c.-312-28379= XM_005273032.1:c.-312-28379T>A XM_005273032.1:c.-312-28379T>C XM_005273032.1:c.-312-28379T>G
CHRM3 transcript variant X3 XM_005273033.1:c.-250+58096= XM_005273033.1:c.-250+58096T>A XM_005273033.1:c.-250+58096T>C XM_005273033.1:c.-250+58096T>G
CHRM3 transcript variant X4 XM_011544043.2:c.-645-28379= XM_011544043.2:c.-645-28379T>A XM_011544043.2:c.-645-28379T>C XM_011544043.2:c.-645-28379T>G
CHRM3 transcript variant X5 XM_011544044.2:c.-416-28379= XM_011544044.2:c.-416-28379T>A XM_011544044.2:c.-416-28379T>C XM_011544044.2:c.-416-28379T>G
CHRM3 transcript variant X10 XM_011544047.2:c.-185-28379= XM_011544047.2:c.-185-28379T>A XM_011544047.2:c.-185-28379T>C XM_011544047.2:c.-185-28379T>G
CHRM3 transcript variant X2 XM_017000152.2:c.-312-28379= XM_017000152.2:c.-312-28379T>A XM_017000152.2:c.-312-28379T>C XM_017000152.2:c.-312-28379T>G
CHRM3 transcript variant X9 XM_017000154.1:c.-312-28379= XM_017000154.1:c.-312-28379T>A XM_017000154.1:c.-312-28379T>C XM_017000154.1:c.-312-28379T>G
CHRM3 transcript variant X12 XM_017000157.2:c.-313+13640= XM_017000157.2:c.-313+13640T>A XM_017000157.2:c.-313+13640T>C XM_017000157.2:c.-313+13640T>G
CHRM3 transcript variant X14 XM_017000159.1:c.-123+58096= XM_017000159.1:c.-123+58096T>A XM_017000159.1:c.-123+58096T>C XM_017000159.1:c.-123+58096T>G
CHRM3 transcript variant X17 XM_017000162.1:c.-185-28379= XM_017000162.1:c.-185-28379T>A XM_017000162.1:c.-185-28379T>C XM_017000162.1:c.-185-28379T>G
Help

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#.

68 SubSNP, 18 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_SNP ss18069720 Feb 27, 2004 (120)
2 SC_SNP ss18243023 Feb 27, 2004 (120)
3 SSAHASNP ss20429443 Apr 05, 2004 (121)
4 PERLEGEN ss23867331 Sep 20, 2004 (123)
5 ABI ss41282528 Mar 14, 2006 (126)
6 AFFY ss76805327 Dec 07, 2007 (129)
7 HGSV ss78066578 Dec 07, 2007 (129)
8 HGSV ss81164412 Dec 15, 2007 (130)
9 BCMHGSC_JDW ss88028195 Mar 23, 2008 (129)
10 HUMANGENOME_JCVI ss98014863 Feb 05, 2009 (130)
11 BGI ss102836976 Dec 01, 2009 (131)
12 KRIBB_YJKIM ss105018214 Feb 05, 2009 (130)
13 1000GENOMES ss109081821 Jan 23, 2009 (130)
14 ENSEMBL ss138182905 Dec 01, 2009 (131)
15 ENSEMBL ss139020339 Dec 01, 2009 (131)
16 GMI ss156489557 Dec 01, 2009 (131)
17 COMPLETE_GENOMICS ss165515449 Jul 04, 2010 (132)
18 BCM-HGSC-SUB ss205393328 Jul 04, 2010 (132)
19 1000GENOMES ss210778300 Jul 14, 2010 (132)
20 1000GENOMES ss218971766 Jul 14, 2010 (132)
21 1000GENOMES ss230970077 Jul 14, 2010 (132)
22 1000GENOMES ss238570802 Jul 15, 2010 (132)
23 BL ss253916529 May 09, 2011 (134)
24 GMI ss276284721 May 04, 2012 (137)
25 GMI ss284258683 Apr 25, 2013 (138)
26 PJP ss290768259 May 09, 2011 (134)
27 TISHKOFF ss555245695 Apr 25, 2013 (138)
28 SSMP ss648820003 Apr 25, 2013 (138)
29 EVA-GONL ss976319397 Aug 21, 2014 (142)
30 JMKIDD_LAB ss1068733804 Aug 21, 2014 (142)
31 1000GENOMES ss1295294993 Aug 21, 2014 (142)
32 DDI ss1426163588 Apr 01, 2015 (144)
33 EVA_GENOME_DK ss1574792437 Apr 01, 2015 (144)
34 EVA_DECODE ss1585722992 Apr 01, 2015 (144)
35 EVA_UK10K_ALSPAC ss1602486575 Apr 01, 2015 (144)
36 EVA_UK10K_TWINSUK ss1645480608 Apr 01, 2015 (144)
37 EVA_SVP ss1712418891 Apr 01, 2015 (144)
38 WEILL_CORNELL_DGM ss1919540832 Feb 12, 2016 (147)
39 GENOMED ss1967015029 Jul 19, 2016 (147)
40 JJLAB ss2020297863 Sep 14, 2016 (149)
41 USC_VALOUEV ss2148335637 Nov 08, 2017 (151)
42 HUMAN_LONGEVITY ss2171414754 Dec 20, 2016 (150)
43 TOPMED ss2334066629 Dec 20, 2016 (150)
44 SYSTEMSBIOZJU ss2624662164 Nov 08, 2017 (151)
45 GRF ss2698338720 Nov 08, 2017 (151)
46 GNOMAD ss2768029352 Nov 08, 2017 (151)
47 AFFY ss2985543631 Nov 08, 2017 (151)
48 SWEGEN ss2988719764 Nov 08, 2017 (151)
49 BIOINF_KMB_FNS_UNIBA ss3023910833 Nov 08, 2017 (151)
50 TOPMED ss3107541840 Nov 08, 2017 (151)
51 CSHL ss3343990833 Nov 08, 2017 (151)
52 URBANLAB ss3646923651 Oct 11, 2018 (152)
53 EGCUT_WGS ss3656680163 Jul 12, 2019 (153)
54 EVA_DECODE ss3688954244 Jul 12, 2019 (153)
55 ACPOP ss3728008838 Jul 12, 2019 (153)
56 EVA ss3747540349 Jul 12, 2019 (153)
57 PACBIO ss3783733895 Jul 12, 2019 (153)
58 PACBIO ss3789339145 Jul 12, 2019 (153)
59 PACBIO ss3794211597 Jul 12, 2019 (153)
60 KHV_HUMAN_GENOMES ss3800543107 Jul 12, 2019 (153)
61 EVA ss3826731596 Apr 25, 2020 (154)
62 EVA ss3836768524 Apr 25, 2020 (154)
63 EVA ss3842181418 Apr 25, 2020 (154)
64 SGDP_PRJ ss3851238568 Apr 25, 2020 (154)
65 KRGDB ss3896597498 Apr 25, 2020 (154)
66 KOGIC ss3946825352 Apr 25, 2020 (154)
67 TOPMED ss4489150565 Apr 25, 2021 (155)
68 TOMMO_GENOMICS ss5149170739 Apr 25, 2021 (155)
69 1000Genomes NC_000001.10 - 239767145 Oct 11, 2018 (152)
70 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 239767145 Oct 11, 2018 (152)
71 Genetic variation in the Estonian population NC_000001.10 - 239767145 Oct 11, 2018 (152)
72 The Danish reference pan genome NC_000001.10 - 239767145 Apr 25, 2020 (154)
73 gnomAD - Genomes NC_000001.11 - 239603845 Apr 25, 2021 (155)
74 Genome of the Netherlands Release 5 NC_000001.10 - 239767145 Apr 25, 2020 (154)
75 HapMap NC_000001.11 - 239603845 Apr 25, 2020 (154)
76 KOREAN population from KRGDB NC_000001.10 - 239767145 Apr 25, 2020 (154)
77 Korean Genome Project NC_000001.11 - 239603845 Apr 25, 2020 (154)
78 Northern Sweden NC_000001.10 - 239767145 Jul 12, 2019 (153)
79 Qatari NC_000001.10 - 239767145 Apr 25, 2020 (154)
80 SGDP_PRJ NC_000001.10 - 239767145 Apr 25, 2020 (154)
81 Siberian NC_000001.10 - 239767145 Apr 25, 2020 (154)
82 8.3KJPN NC_000001.10 - 239767145 Apr 25, 2021 (155)
83 TopMed NC_000001.11 - 239603845 Apr 25, 2021 (155)
84 UK 10K study - Twins NC_000001.10 - 239767145 Oct 11, 2018 (152)
85 A Vietnamese Genetic Variation Database NC_000001.10 - 239767145 Jul 12, 2019 (153)
86 ALFA NC_000001.11 - 239603845 Apr 25, 2021 (155)
Help

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)
rs58949378 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
3774892, ss3896597498 NC_000001.10:239767144:T:A NC_000001.11:239603844:T:A (self)
3774892, ss3896597498 NC_000001.10:239767144:T:C NC_000001.11:239603844:T:C (self)
ss78066578, ss81164412 NC_000001.8:236093185:T:G NC_000001.11:239603844:T:G (self)
ss88028195, ss109081821, ss165515449, ss205393328, ss210778300, ss253916529, ss276284721, ss284258683, ss290768259, ss1585722992, ss1712418891 NC_000001.9:237833767:T:G NC_000001.11:239603844:T:G (self)
6173571, 3420535, 2418411, 1955760, 1497793, 3774892, 1293703, 1582762, 3255548, 851991, 7140046, 3420535, 746007, ss218971766, ss230970077, ss238570802, ss555245695, ss648820003, ss976319397, ss1068733804, ss1295294993, ss1426163588, ss1574792437, ss1602486575, ss1645480608, ss1919540832, ss1967015029, ss2020297863, ss2148335637, ss2334066629, ss2624662164, ss2698338720, ss2768029352, ss2985543631, ss2988719764, ss3343990833, ss3656680163, ss3728008838, ss3747540349, ss3783733895, ss3789339145, ss3794211597, ss3826731596, ss3836768524, ss3851238568, ss3896597498, ss5149170739 NC_000001.10:239767144:T:G NC_000001.11:239603844:T:G (self)
44193146, 303351, 3203353, 33164723, 52756900, 6763418369, ss2171414754, ss3023910833, ss3107541840, ss3646923651, ss3688954244, ss3800543107, ss3842181418, ss3946825352, ss4489150565 NC_000001.11:239603844:T:G NC_000001.11:239603844:T:G (self)
ss18069720, ss18243023, ss20429443 NT_004836.15:4524933:T:G NC_000001.11:239603844:T:G (self)
ss23867331, ss41282528, ss76805327, ss98014863, ss102836976, ss105018214, ss138182905, ss139020339, ss156489557 NT_167186.1:33284923:T:G NC_000001.11:239603844:T:G (self)
Help

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

No publications for rs10925924

Help

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.

Software version is: 2.0.1.post596+ae089ad