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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs61731141

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr12:6355778 (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
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.016272 (4307/264690, TOPMED)
A=0.007455 (1875/251496, GnomAD_exome)
A=0.004279 (938/219192, ALFA) (+ 18 more)
A=0.015087 (2116/140256, GnomAD)
A=0.008533 (1036/121412, ExAC)
A=0.02515 (1979/78700, PAGE_STUDY)
A=0.00060 (17/28258, 14KJPN)
A=0.00054 (9/16760, 8.3KJPN)
A=0.01707 (222/13006, GO-ESP)
A=0.0208 (133/6404, 1000G_30x)
A=0.0186 (93/5008, 1000G)
A=0.0002 (1/4480, Estonian)
A=0.0003 (1/3854, ALSPAC)
A=0.0003 (1/3708, TWINSUK)
A=0.0017 (5/2922, KOREAN)
A=0.0011 (2/1832, Korea1K)
A=0.001 (1/998, GoNL)
A=0.003 (2/792, PRJEB37584)
A=0.002 (1/534, MGP)
A=0.019 (4/216, Qatari)
G=0.46 (13/28, SGDP_PRJ)
Clinical Significance
Reported in ClinVar
Gene : Consequence
SCNN1A : Synonymous Variant
LOC107984500 : Non Coding Transcript 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 235698 G=0.994909 A=0.005091
European Sub 195138 G=0.997863 A=0.002137
African Sub 12662 G=0.95640 A=0.04360
African Others Sub 454 G=0.943 A=0.057
African American Sub 12208 G=0.95691 A=0.04309
Asian Sub 6366 G=0.9928 A=0.0072
East Asian Sub 4516 G=0.9973 A=0.0027
Other Asian Sub 1850 G=0.9816 A=0.0184
Latin American 1 Sub 818 G=0.982 A=0.018
Latin American 2 Sub 1058 G=0.9953 A=0.0047
South Asian Sub 296 G=0.986 A=0.014
Other Sub 19360 G=0.99168 A=0.00832


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 G=0.983728 A=0.016272
gnomAD - Exomes Global Study-wide 251496 G=0.992545 A=0.007455
gnomAD - Exomes European Sub 135418 G=0.998516 A=0.001484
gnomAD - Exomes Asian Sub 49010 G=0.98694 A=0.01306
gnomAD - Exomes American Sub 34592 G=0.99722 A=0.00278
gnomAD - Exomes African Sub 16256 G=0.95251 A=0.04749
gnomAD - Exomes Ashkenazi Jewish Sub 10080 G=0.98700 A=0.01300
gnomAD - Exomes Other Sub 6140 G=0.9943 A=0.0057
Allele Frequency Aggregator Total Global 219192 G=0.995721 A=0.004279
Allele Frequency Aggregator European Sub 184922 G=0.997821 A=0.002179
Allele Frequency Aggregator Other Sub 17908 G=0.99224 A=0.00776
Allele Frequency Aggregator African Sub 7824 G=0.9583 A=0.0417
Allele Frequency Aggregator Asian Sub 6366 G=0.9928 A=0.0072
Allele Frequency Aggregator Latin American 2 Sub 1058 G=0.9953 A=0.0047
Allele Frequency Aggregator Latin American 1 Sub 818 G=0.982 A=0.018
Allele Frequency Aggregator South Asian Sub 296 G=0.986 A=0.014
gnomAD - Genomes Global Study-wide 140256 G=0.984913 A=0.015087
gnomAD - Genomes European Sub 75944 G=0.99854 A=0.00146
gnomAD - Genomes African Sub 42038 G=0.95571 A=0.04429
gnomAD - Genomes American Sub 13664 G=0.99393 A=0.00607
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=0.9898 A=0.0102
gnomAD - Genomes East Asian Sub 3134 G=0.9990 A=0.0010
gnomAD - Genomes Other Sub 2154 G=0.9893 A=0.0107
ExAC Global Study-wide 121412 G=0.991467 A=0.008533
ExAC Europe Sub 73354 G=0.99783 A=0.00217
ExAC Asian Sub 25166 G=0.98593 A=0.01407
ExAC American Sub 11578 G=0.99732 A=0.00268
ExAC African Sub 10406 G=0.95349 A=0.04651
ExAC Other Sub 908 G=0.991 A=0.009
The PAGE Study Global Study-wide 78700 G=0.97485 A=0.02515
The PAGE Study AfricanAmerican Sub 32516 G=0.95694 A=0.04306
The PAGE Study Mexican Sub 10810 G=0.99713 A=0.00287
The PAGE Study Asian Sub 8318 G=0.9992 A=0.0008
The PAGE Study PuertoRican Sub 7916 G=0.9874 A=0.0126
The PAGE Study NativeHawaiian Sub 4534 G=0.9455 A=0.0545
The PAGE Study Cuban Sub 4230 G=0.9910 A=0.0090
The PAGE Study Dominican Sub 3828 G=0.9739 A=0.0261
The PAGE Study CentralAmerican Sub 2450 G=0.9927 A=0.0073
The PAGE Study SouthAmerican Sub 1982 G=0.9950 A=0.0050
The PAGE Study NativeAmerican Sub 1260 G=0.9937 A=0.0063
The PAGE Study SouthAsian Sub 856 G=0.977 A=0.023
14KJPN JAPANESE Study-wide 28258 G=0.99940 A=0.00060
8.3KJPN JAPANESE Study-wide 16760 G=0.99946 A=0.00054
GO Exome Sequencing Project Global Study-wide 13006 G=0.98293 A=0.01707
GO Exome Sequencing Project European American Sub 8600 G=0.9984 A=0.0016
GO Exome Sequencing Project African American Sub 4406 G=0.9528 A=0.0472
1000Genomes_30x Global Study-wide 6404 G=0.9792 A=0.0208
1000Genomes_30x African Sub 1786 G=0.9418 A=0.0582
1000Genomes_30x Europe Sub 1266 G=0.9961 A=0.0039
1000Genomes_30x South Asian Sub 1202 G=0.9842 A=0.0158
1000Genomes_30x East Asian Sub 1170 G=1.0000 A=0.0000
1000Genomes_30x American Sub 980 G=0.995 A=0.005
1000Genomes Global Study-wide 5008 G=0.9814 A=0.0186
1000Genomes African Sub 1322 G=0.9455 A=0.0545
1000Genomes East Asian Sub 1008 G=1.0000 A=0.0000
1000Genomes Europe Sub 1006 G=0.9960 A=0.0040
1000Genomes South Asian Sub 978 G=0.986 A=0.014
1000Genomes American Sub 694 G=0.996 A=0.004
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.9998 A=0.0002
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.9997 A=0.0003
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.9997 A=0.0003
KOREAN population from KRGDB KOREAN Study-wide 2922 G=0.9983 A=0.0017
Korean Genome Project KOREAN Study-wide 1832 G=0.9989 A=0.0011
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.999 A=0.001
CNV burdens in cranial meningiomas Global Study-wide 792 G=0.997 A=0.003
CNV burdens in cranial meningiomas CRM Sub 792 G=0.997 A=0.003
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 G=0.998 A=0.002
Qatari Global Study-wide 216 G=0.981 A=0.019
SGDP_PRJ Global Study-wide 28 G=0.46 A=0.54
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.p14 chr 12 NC_000012.12:g.6355778G>A
GRCh37.p13 chr 12 NC_000012.11:g.6464944G>A
SCNN1A RefSeqGene NG_011945.2:g.26580C>T
Gene: SCNN1A, sodium channel epithelial 1 subunit alpha (minus strand)
Molecule type Change Amino acid[Codon] SO Term
SCNN1A transcript variant 1 NM_001038.6:c.978C>T N [AAC] > N [AAT] Coding Sequence Variant
amiloride-sensitive sodium channel subunit alpha isoform 1 NP_001029.1:p.Asn326= N (Asn) > N (Asn) Synonymous Variant
SCNN1A transcript variant 2 NM_001159576.2:c.1155C>T N [AAC] > N [AAT] Coding Sequence Variant
amiloride-sensitive sodium channel subunit alpha isoform 2 NP_001153048.1:p.Asn385= N (Asn) > N (Asn) Synonymous Variant
SCNN1A transcript variant 3 NM_001159575.2:c.1047C>T N [AAC] > N [AAT] Coding Sequence Variant
amiloride-sensitive sodium channel subunit alpha isoform 3 NP_001153047.1:p.Asn349= N (Asn) > N (Asn) Synonymous Variant
Gene: LOC107984500, uncharacterized LOC107984500 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
LOC107984500 transcript XR_007063191.1:n.550G>A N/A Non Coding Transcript 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.

Allele: A (allele ID: 318280 )
ClinVar Accession Disease Names Clinical Significance
RCV000266859.3 Autosomal recessive pseudohypoaldosteronism type 1 Benign
RCV000359208.3 Bronchiectasis with or without elevated sweat chloride 2 Benign
RCV000602567.3 not specified Benign
RCV000959256.6 not provided Benign-Likely-Benign
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 G= A
GRCh38.p14 chr 12 NC_000012.12:g.6355778= NC_000012.12:g.6355778G>A
GRCh37.p13 chr 12 NC_000012.11:g.6464944= NC_000012.11:g.6464944G>A
SCNN1A RefSeqGene NG_011945.2:g.26580= NG_011945.2:g.26580C>T
SCNN1A transcript variant 1 NM_001038.6:c.978= NM_001038.6:c.978C>T
SCNN1A transcript variant 1 NM_001038.5:c.978= NM_001038.5:c.978C>T
SCNN1A transcript variant 2 NM_001159576.2:c.1155= NM_001159576.2:c.1155C>T
SCNN1A transcript variant 2 NM_001159576.1:c.1155= NM_001159576.1:c.1155C>T
SCNN1A transcript variant 3 NM_001159575.2:c.1047= NM_001159575.2:c.1047C>T
SCNN1A transcript variant 3 NM_001159575.1:c.1047= NM_001159575.1:c.1047C>T
LOC107984500 transcript XR_007063191.1:n.550= XR_007063191.1:n.550G>A
amiloride-sensitive sodium channel subunit alpha isoform 1 NP_001029.1:p.Asn326= NP_001029.1:p.Asn326=
amiloride-sensitive sodium channel subunit alpha isoform 2 NP_001153048.1:p.Asn385= NP_001153048.1:p.Asn385=
amiloride-sensitive sodium channel subunit alpha isoform 3 NP_001153047.1:p.Asn349= NP_001153047.1:p.Asn349=
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#.

79 SubSNP, 21 Frequency, 4 ClinVar submissions
No Submitter Submission ID Date (Build)
1 CORNELL ss86244006 Mar 23, 2008 (129)
2 APPLERA_GI ss95211401 Mar 25, 2008 (129)
3 RSG_JCVI ss107932154 Feb 05, 2009 (130)
4 SEATTLESEQ ss159725464 Dec 01, 2009 (131)
5 BUSHMAN ss203499829 Jul 04, 2010 (132)
6 1000GENOMES ss225588376 Jul 14, 2010 (132)
7 NHLBI-ESP ss342347773 May 09, 2011 (134)
8 ILLUMINA ss481806417 May 04, 2012 (137)
9 ILLUMINA ss483093889 May 04, 2012 (137)
10 1000GENOMES ss491035161 May 04, 2012 (137)
11 EXOME_CHIP ss491463080 May 04, 2012 (137)
12 CLINSEQ_SNP ss491658808 May 04, 2012 (137)
13 ILLUMINA ss534398527 Sep 08, 2015 (146)
14 ILLUMINA ss779308629 Sep 08, 2015 (146)
15 ILLUMINA ss780907168 Sep 08, 2015 (146)
16 ILLUMINA ss781573757 Sep 08, 2015 (146)
17 ILLUMINA ss783594585 Sep 08, 2015 (146)
18 ILLUMINA ss834775990 Sep 08, 2015 (146)
19 JMKIDD_LAB ss974482309 Aug 21, 2014 (142)
20 EVA-GONL ss989200277 Aug 21, 2014 (142)
21 JMKIDD_LAB ss1067530863 Aug 21, 2014 (142)
22 JMKIDD_LAB ss1078221593 Aug 21, 2014 (142)
23 1000GENOMES ss1343862821 Aug 21, 2014 (142)
24 EVA_UK10K_ALSPAC ss1627948496 Apr 01, 2015 (144)
25 EVA_UK10K_TWINSUK ss1670942529 Apr 01, 2015 (144)
26 EVA_EXAC ss1690754564 Apr 01, 2015 (144)
27 EVA_MGP ss1711317827 Apr 01, 2015 (144)
28 ILLUMINA ss1752077030 Sep 08, 2015 (146)
29 HAMMER_LAB ss1807102529 Sep 08, 2015 (146)
30 ILLUMINA ss1917869843 Feb 12, 2016 (147)
31 WEILL_CORNELL_DGM ss1932562181 Feb 12, 2016 (147)
32 ILLUMINA ss1946329896 Feb 12, 2016 (147)
33 ILLUMINA ss1959409435 Feb 12, 2016 (147)
34 HUMAN_LONGEVITY ss2187532604 Dec 20, 2016 (150)
35 ILLUMINA ss2632920611 Nov 08, 2017 (151)
36 GNOMAD ss2739576650 Nov 08, 2017 (151)
37 GNOMAD ss2748796544 Nov 08, 2017 (151)
38 GNOMAD ss2906940104 Nov 08, 2017 (151)
39 AFFY ss2984966069 Nov 08, 2017 (151)
40 ILLUMINA ss3021402334 Nov 08, 2017 (151)
41 ILLUMINA ss3626807594 Oct 12, 2018 (152)
42 ILLUMINA ss3626807595 Oct 12, 2018 (152)
43 ILLUMINA ss3630932511 Oct 12, 2018 (152)
44 ILLUMINA ss3634488716 Oct 12, 2018 (152)
45 ILLUMINA ss3640196050 Oct 12, 2018 (152)
46 ILLUMINA ss3644582836 Oct 12, 2018 (152)
47 OMUKHERJEE_ADBS ss3646436539 Oct 12, 2018 (152)
48 ILLUMINA ss3651774483 Oct 12, 2018 (152)
49 ILLUMINA ss3653738362 Oct 12, 2018 (152)
50 EGCUT_WGS ss3676473086 Jul 13, 2019 (153)
51 EVA_DECODE ss3693041609 Jul 13, 2019 (153)
52 ILLUMINA ss3725299975 Jul 13, 2019 (153)
53 ILLUMINA ss3744391115 Jul 13, 2019 (153)
54 ILLUMINA ss3744789440 Jul 13, 2019 (153)
55 EVA ss3750097891 Jul 13, 2019 (153)
56 PAGE_CC ss3771671785 Jul 13, 2019 (153)
57 ILLUMINA ss3772289031 Jul 13, 2019 (153)
58 KHV_HUMAN_GENOMES ss3815412826 Jul 13, 2019 (153)
59 EVA ss3824697647 Apr 26, 2020 (154)
60 EVA ss3825815188 Apr 26, 2020 (154)
61 SGDP_PRJ ss3877610367 Apr 26, 2020 (154)
62 KRGDB ss3926110165 Apr 26, 2020 (154)
63 KOGIC ss3971206609 Apr 26, 2020 (154)
64 FSA-LAB ss3984019645 Apr 26, 2021 (155)
65 EVA ss3984661666 Apr 26, 2021 (155)
66 EVA ss3986556110 Apr 26, 2021 (155)
67 TOPMED ss4907518491 Apr 26, 2021 (155)
68 TOMMO_GENOMICS ss5204895692 Apr 26, 2021 (155)
69 EVA ss5237659264 Oct 16, 2022 (156)
70 1000G_HIGH_COVERAGE ss5289680363 Oct 16, 2022 (156)
71 EVA ss5403700961 Oct 16, 2022 (156)
72 HUGCELL_USP ss5484586908 Oct 16, 2022 (156)
73 1000G_HIGH_COVERAGE ss5586544726 Oct 16, 2022 (156)
74 SANFORD_IMAGENETICS ss5652518003 Oct 16, 2022 (156)
75 TOMMO_GENOMICS ss5753637576 Oct 16, 2022 (156)
76 EVA ss5837538369 Oct 16, 2022 (156)
77 EVA ss5847658480 Oct 16, 2022 (156)
78 EVA ss5903150839 Oct 16, 2022 (156)
79 EVA ss5943867819 Oct 16, 2022 (156)
80 1000Genomes NC_000012.11 - 6464944 Oct 12, 2018 (152)
81 1000Genomes_30x NC_000012.12 - 6355778 Oct 16, 2022 (156)
82 The Avon Longitudinal Study of Parents and Children NC_000012.11 - 6464944 Oct 12, 2018 (152)
83 Genetic variation in the Estonian population NC_000012.11 - 6464944 Oct 12, 2018 (152)
84 ExAC NC_000012.11 - 6464944 Oct 12, 2018 (152)
85 gnomAD - Genomes NC_000012.12 - 6355778 Apr 26, 2021 (155)
86 gnomAD - Exomes NC_000012.11 - 6464944 Jul 13, 2019 (153)
87 GO Exome Sequencing Project NC_000012.11 - 6464944 Oct 12, 2018 (152)
88 Genome of the Netherlands Release 5 NC_000012.11 - 6464944 Apr 26, 2020 (154)
89 KOREAN population from KRGDB NC_000012.11 - 6464944 Apr 26, 2020 (154)
90 Korean Genome Project NC_000012.12 - 6355778 Apr 26, 2020 (154)
91 Medical Genome Project healthy controls from Spanish population NC_000012.11 - 6464944 Apr 26, 2020 (154)
92 The PAGE Study NC_000012.12 - 6355778 Jul 13, 2019 (153)
93 CNV burdens in cranial meningiomas NC_000012.11 - 6464944 Apr 26, 2021 (155)
94 Qatari NC_000012.11 - 6464944 Apr 26, 2020 (154)
95 SGDP_PRJ NC_000012.11 - 6464944 Apr 26, 2020 (154)
96 8.3KJPN NC_000012.11 - 6464944 Apr 26, 2021 (155)
97 14KJPN NC_000012.12 - 6355778 Oct 16, 2022 (156)
98 TopMed NC_000012.12 - 6355778 Apr 26, 2021 (155)
99 UK 10K study - Twins NC_000012.11 - 6464944 Oct 12, 2018 (152)
100 ALFA NC_000012.12 - 6355778 Apr 26, 2021 (155)
101 ClinVar RCV000266859.3 Oct 16, 2022 (156)
102 ClinVar RCV000359208.3 Oct 16, 2022 (156)
103 ClinVar RCV000602567.3 Oct 16, 2022 (156)
104 ClinVar RCV000959256.6 Oct 16, 2022 (156)
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).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss203499829, ss483093889, ss491658808 NC_000012.10:6335204:G:A NC_000012.12:6355777:G:A (self)
56476166, 31364881, 22211334, 1039017, 8800943, 1155145, 13991126, 33287559, 433587, 211157, 14604111, 29627347, 62864999, 31364881, ss225588376, ss342347773, ss481806417, ss491035161, ss491463080, ss534398527, ss779308629, ss780907168, ss781573757, ss783594585, ss834775990, ss974482309, ss989200277, ss1067530863, ss1078221593, ss1343862821, ss1627948496, ss1670942529, ss1690754564, ss1711317827, ss1752077030, ss1807102529, ss1917869843, ss1932562181, ss1946329896, ss1959409435, ss2632920611, ss2739576650, ss2748796544, ss2906940104, ss2984966069, ss3021402334, ss3626807594, ss3626807595, ss3630932511, ss3634488716, ss3640196050, ss3644582836, ss3646436539, ss3651774483, ss3653738362, ss3676473086, ss3744391115, ss3744789440, ss3750097891, ss3772289031, ss3824697647, ss3825815188, ss3877610367, ss3926110165, ss3984019645, ss3984661666, ss3986556110, ss5204895692, ss5403700961, ss5652518003, ss5837538369, ss5847658480, ss5943867819 NC_000012.11:6464943:G:A NC_000012.12:6355777:G:A (self)
RCV000266859.3, RCV000359208.3, RCV000602567.3, RCV000959256.6, 74070661, 398258719, 27584610, 893254, 87474680, 123064148, 4693788855, ss2187532604, ss3693041609, ss3725299975, ss3771671785, ss3815412826, ss3971206609, ss4907518491, ss5237659264, ss5289680363, ss5484586908, ss5586544726, ss5753637576, ss5903150839 NC_000012.12:6355777:G:A NC_000012.12:6355777:G:A (self)
ss86244006, ss95211401, ss107932154, ss159725464 NT_009759.16:6404943:G:A NC_000012.12:6355777:G:A (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 rs61731141

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.post761+d5e8e07