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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.

rs2544677

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr5:87103445 (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
G=0.153168 (40542/264690, TOPMED)
G=0.00011 (3/28258, 14KJPN)
G=0.00006 (1/16760, 8.3KJPN) (+ 14 more)
G=0.2952 (2267/7680, ALFA)
G=0.0920 (589/6404, 1000G_30x)
G=0.0925 (463/5008, 1000G)
G=0.2701 (1210/4480, Estonian)
G=0.0007 (2/2930, KOREAN)
G=0.0000 (0/1832, Korea1K)
G=0.1265 (207/1636, HapMap)
G=0.206 (206/998, GoNL)
G=0.230 (138/600, NorthernSweden)
G=0.082 (45/550, SGDP_PRJ)
G=0.282 (61/216, Qatari)
G=0.005 (1/212, Vietnamese)
G=0.22 (12/54, Siberian)
G=0.25 (10/40, GENOME_DK)
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 7680 G=0.2952 A=0.0000, C=0.7048, T=0.0000
European Sub 7210 G=0.2996 A=0.0000, C=0.7004, T=0.0000
African Sub 174 G=0.155 A=0.000, C=0.845, T=0.000
African Others Sub 6 G=0.2 A=0.0, C=0.8, T=0.0
African American Sub 168 G=0.155 A=0.000, C=0.845, T=0.000
Asian Sub 6 G=0.0 A=0.0, C=1.0, T=0.0
East Asian Sub 4 G=0.0 A=0.0, C=1.0, T=0.0
Other Asian Sub 2 G=0.0 A=0.0, C=1.0, T=0.0
Latin American 1 Sub 14 G=0.86 A=0.00, C=0.14, T=0.00
Latin American 2 Sub 20 G=0.30 A=0.00, C=0.70, T=0.00
South Asian Sub 4 G=0.5 A=0.0, C=0.5, T=0.0
Other Sub 252 G=0.238 A=0.000, C=0.762, T=0.000


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=0.153168 C=0.846832
14KJPN JAPANESE Study-wide 28258 G=0.00011 C=0.99989
8.3KJPN JAPANESE Study-wide 16760 G=0.00006 C=0.99994
Allele Frequency Aggregator Total Global 7680 G=0.2952 A=0.0000, C=0.7048, T=0.0000
Allele Frequency Aggregator European Sub 7210 G=0.2996 A=0.0000, C=0.7004, T=0.0000
Allele Frequency Aggregator Other Sub 252 G=0.238 A=0.000, C=0.762, T=0.000
Allele Frequency Aggregator African Sub 174 G=0.155 A=0.000, C=0.845, T=0.000
Allele Frequency Aggregator Latin American 2 Sub 20 G=0.30 A=0.00, C=0.70, T=0.00
Allele Frequency Aggregator Latin American 1 Sub 14 G=0.86 A=0.00, C=0.14, T=0.00
Allele Frequency Aggregator Asian Sub 6 G=0.0 A=0.0, C=1.0, T=0.0
Allele Frequency Aggregator South Asian Sub 4 G=0.5 A=0.0, C=0.5, T=0.0
1000Genomes_30x Global Study-wide 6404 G=0.0920 A=0.0072, C=0.9008
1000Genomes_30x African Sub 1786 G=0.0398 A=0.0224, C=0.9378
1000Genomes_30x Europe Sub 1266 G=0.2259 A=0.0000, C=0.7741
1000Genomes_30x South Asian Sub 1202 G=0.1082 A=0.0000, C=0.8918
1000Genomes_30x East Asian Sub 1170 G=0.0043 A=0.0000, C=0.9957
1000Genomes_30x American Sub 980 G=0.099 A=0.006, C=0.895
1000Genomes Global Study-wide 5008 G=0.0925 A=0.0068, C=0.9008
1000Genomes African Sub 1322 G=0.0469 A=0.0227, C=0.9304
1000Genomes East Asian Sub 1008 G=0.0040 A=0.0000, C=0.9960
1000Genomes Europe Sub 1006 G=0.2286 A=0.0000, C=0.7714
1000Genomes South Asian Sub 978 G=0.104 A=0.000, C=0.896
1000Genomes American Sub 694 G=0.094 A=0.006, C=0.901
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.2701 C=0.7299
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.0007 A=0.0000, C=0.9993
Korean Genome Project KOREAN Study-wide 1832 G=0.0000 C=1.0000
HapMap Global Study-wide 1636 G=0.1265 C=0.8735
HapMap African Sub 690 G=0.091 C=0.909
HapMap American Sub 598 G=0.176 C=0.824
HapMap Europe Sub 176 G=0.216 C=0.784
HapMap Asian Sub 172 G=0.006 C=0.994
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.206 C=0.794
Northern Sweden ACPOP Study-wide 600 G=0.230 C=0.770
SGDP_PRJ Global Study-wide 550 G=0.082 A=0.007, C=0.911
Qatari Global Study-wide 216 G=0.282 C=0.718
A Vietnamese Genetic Variation Database Global Study-wide 212 G=0.005 C=0.995
Siberian Global Study-wide 54 G=0.22 C=0.78
The Danish reference pan genome Danish Study-wide 40 G=0.25 C=0.75
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 5 NC_000005.10:g.87103445G>A
GRCh38.p14 chr 5 NC_000005.10:g.87103445G>C
GRCh38.p14 chr 5 NC_000005.10:g.87103445G>T
GRCh37.p13 chr 5 NC_000005.9:g.86399262G>A
GRCh37.p13 chr 5 NC_000005.9:g.86399262G>C
GRCh37.p13 chr 5 NC_000005.9:g.86399262G>T
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
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 C T
GRCh38.p14 chr 5 NC_000005.10:g.87103445= NC_000005.10:g.87103445G>A NC_000005.10:g.87103445G>C NC_000005.10:g.87103445G>T
GRCh37.p13 chr 5 NC_000005.9:g.86399262= NC_000005.9:g.86399262G>A NC_000005.9:g.86399262G>C NC_000005.9:g.86399262G>T
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#.

113 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss3568268 Sep 28, 2001 (100)
2 BCM_SSAHASNP ss10228035 Jul 11, 2003 (116)
3 WI_SSAHASNP ss11731065 Jul 11, 2003 (116)
4 CSHL-HAPMAP ss17858407 Feb 27, 2004 (120)
5 SSAHASNP ss22290239 Apr 05, 2004 (121)
6 PERLEGEN ss24621565 Sep 20, 2004 (123)
7 ABI ss44637787 Mar 13, 2006 (126)
8 AFFY ss66069951 Nov 29, 2006 (127)
9 PERLEGEN ss68941482 May 16, 2007 (127)
10 AFFY ss75998366 Dec 07, 2007 (129)
11 KRIBB_YJKIM ss81815796 Dec 14, 2007 (130)
12 BCMHGSC_JDW ss93165524 Mar 24, 2008 (129)
13 HUMANGENOME_JCVI ss98631114 Feb 06, 2009 (130)
14 BGI ss105935697 Feb 06, 2009 (130)
15 1000GENOMES ss109198442 Jan 23, 2009 (130)
16 1000GENOMES ss112147770 Jan 25, 2009 (130)
17 ILLUMINA-UK ss116702932 Feb 14, 2009 (130)
18 ENSEMBL ss143268949 Dec 01, 2009 (131)
19 ENSEMBL ss143579969 Dec 01, 2009 (131)
20 GMI ss155705726 Dec 01, 2009 (131)
21 ILLUMINA ss160557779 Dec 01, 2009 (131)
22 COMPLETE_GENOMICS ss165432756 Jul 04, 2010 (132)
23 COMPLETE_GENOMICS ss166781586 Jul 04, 2010 (132)
24 AFFY ss170199708 Jul 04, 2010 (132)
25 BUSHMAN ss200498938 Jul 04, 2010 (132)
26 BCM-HGSC-SUB ss206921910 Jul 04, 2010 (132)
27 1000GENOMES ss221791955 Jul 14, 2010 (132)
28 1000GENOMES ss233027395 Jul 14, 2010 (132)
29 1000GENOMES ss240181645 Jul 15, 2010 (132)
30 BL ss253603662 May 09, 2011 (134)
31 GMI ss278371541 May 04, 2012 (137)
32 GMI ss285213044 Apr 25, 2013 (138)
33 PJP ss293397488 May 09, 2011 (134)
34 ILLUMINA ss480600079 May 04, 2012 (137)
35 ILLUMINA ss480614321 May 04, 2012 (137)
36 ILLUMINA ss481445302 Sep 08, 2015 (146)
37 ILLUMINA ss485095168 May 04, 2012 (137)
38 ILLUMINA ss537102487 Sep 08, 2015 (146)
39 TISHKOFF ss558524307 Apr 25, 2013 (138)
40 SSMP ss652401149 Apr 25, 2013 (138)
41 ILLUMINA ss779025675 Sep 08, 2015 (146)
42 ILLUMINA ss782993891 Sep 08, 2015 (146)
43 ILLUMINA ss783954591 Sep 08, 2015 (146)
44 ILLUMINA ss832250765 Sep 08, 2015 (146)
45 ILLUMINA ss834488324 Sep 08, 2015 (146)
46 EVA-GONL ss981787930 Aug 21, 2014 (142)
47 JMKIDD_LAB ss1072794668 Aug 21, 2014 (142)
48 1000GENOMES ss1315930559 Aug 21, 2014 (142)
49 1000GENOMES ss1315930560 Aug 21, 2014 (142)
50 DDI ss1430410414 Apr 01, 2015 (144)
51 EVA_GENOME_DK ss1581223497 Apr 01, 2015 (144)
52 EVA_DECODE ss1591305276 Apr 01, 2015 (144)
53 EVA_UK10K_ALSPAC ss1613328407 Apr 01, 2015 (144)
54 EVA_UK10K_ALSPAC ss1613328408 Apr 01, 2015 (144)
55 EVA_UK10K_TWINSUK ss1656322440 Apr 01, 2015 (144)
56 EVA_UK10K_TWINSUK ss1656322441 Apr 01, 2015 (144)
57 EVA_SVP ss1712779404 Apr 01, 2015 (144)
58 ILLUMINA ss1752588419 Sep 08, 2015 (146)
59 HAMMER_LAB ss1803804258 Sep 08, 2015 (146)
60 WEILL_CORNELL_DGM ss1925041769 Feb 12, 2016 (147)
61 GENOMED ss1970138559 Jul 19, 2016 (147)
62 JJLAB ss2023128381 Sep 14, 2016 (149)
63 USC_VALOUEV ss2151284672 Dec 20, 2016 (150)
64 HUMAN_LONGEVITY ss2275435510 Dec 20, 2016 (150)
65 SYSTEMSBIOZJU ss2626061078 Nov 08, 2017 (151)
66 ILLUMINA ss2634304625 Nov 08, 2017 (151)
67 GRF ss2706838176 Nov 08, 2017 (151)
68 GNOMAD ss2827055518 Nov 08, 2017 (151)
69 SWEGEN ss2997280658 Nov 08, 2017 (151)
70 BIOINF_KMB_FNS_UNIBA ss3025349925 Nov 08, 2017 (151)
71 CSHL ss3346484907 Nov 08, 2017 (151)
72 ILLUMINA ss3629278874 Oct 12, 2018 (152)
73 ILLUMINA ss3632230387 Oct 12, 2018 (152)
74 ILLUMINA ss3633380947 Oct 12, 2018 (152)
75 ILLUMINA ss3634101786 Oct 12, 2018 (152)
76 ILLUMINA ss3635010624 Oct 12, 2018 (152)
77 ILLUMINA ss3635783695 Oct 12, 2018 (152)
78 ILLUMINA ss3636722735 Oct 12, 2018 (152)
79 ILLUMINA ss3637536321 Oct 12, 2018 (152)
80 ILLUMINA ss3640717917 Oct 12, 2018 (152)
81 URBANLAB ss3648109473 Oct 12, 2018 (152)
82 EGCUT_WGS ss3665161560 Jul 13, 2019 (153)
83 EVA_DECODE ss3715090961 Jul 13, 2019 (153)
84 EVA_DECODE ss3715090962 Jul 13, 2019 (153)
85 ACPOP ss3732540096 Jul 13, 2019 (153)
86 ILLUMINA ss3745310833 Jul 13, 2019 (153)
87 EVA ss3763681997 Jul 13, 2019 (153)
88 ILLUMINA ss3772804944 Jul 13, 2019 (153)
89 PACBIO ss3785168856 Jul 13, 2019 (153)
90 PACBIO ss3790566099 Jul 13, 2019 (153)
91 PACBIO ss3795442696 Jul 13, 2019 (153)
92 KHV_HUMAN_GENOMES ss3806849844 Jul 13, 2019 (153)
93 EVA ss3829350600 Apr 26, 2020 (154)
94 EVA ss3838149594 Apr 26, 2020 (154)
95 EVA ss3843590909 Apr 26, 2020 (154)
96 SGDP_PRJ ss3862306261 Apr 26, 2020 (154)
97 KRGDB ss3908890770 Apr 26, 2020 (154)
98 KOGIC ss3957077365 Apr 26, 2020 (154)
99 TOPMED ss4667279252 Apr 26, 2021 (155)
100 TOMMO_GENOMICS ss5172713736 Apr 26, 2021 (155)
101 1000G_HIGH_COVERAGE ss5264718334 Oct 13, 2022 (156)
102 1000G_HIGH_COVERAGE ss5264718335 Oct 13, 2022 (156)
103 EVA ss5315066479 Oct 13, 2022 (156)
104 HUGCELL_USP ss5462815143 Oct 13, 2022 (156)
105 HUGCELL_USP ss5462815144 Oct 13, 2022 (156)
106 1000G_HIGH_COVERAGE ss5548753227 Oct 13, 2022 (156)
107 SANFORD_IMAGENETICS ss5638232417 Oct 13, 2022 (156)
108 TOMMO_GENOMICS ss5709384698 Oct 13, 2022 (156)
109 YY_MCH ss5806502890 Oct 13, 2022 (156)
110 EVA ss5835213758 Oct 13, 2022 (156)
111 EVA ss5854899850 Oct 13, 2022 (156)
112 EVA ss5966667946 Oct 13, 2022 (156)
113 EVA ss5980304579 Oct 13, 2022 (156)
114 1000Genomes NC_000005.9 - 86399262 Oct 12, 2018 (152)
115 1000Genomes_30x NC_000005.10 - 87103445 Oct 13, 2022 (156)
116 The Avon Longitudinal Study of Parents and Children

Submission ignored due to conflicting rows:
Row 15324856 (NC_000005.9:86399261:G:G 858/3854, NC_000005.9:86399261:G:C 2996/3854)
Row 15324857 (NC_000005.9:86399261:G:G 3853/3854, NC_000005.9:86399261:G:A 1/3854)

- Oct 12, 2018 (152)
117 The Avon Longitudinal Study of Parents and Children

Submission ignored due to conflicting rows:
Row 15324856 (NC_000005.9:86399261:G:G 858/3854, NC_000005.9:86399261:G:C 2996/3854)
Row 15324857 (NC_000005.9:86399261:G:G 3853/3854, NC_000005.9:86399261:G:A 1/3854)

- Oct 12, 2018 (152)
118 Genetic variation in the Estonian population NC_000005.9 - 86399262 Oct 12, 2018 (152)
119 The Danish reference pan genome NC_000005.9 - 86399262 Apr 26, 2020 (154)
120 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 194860338 (NC_000005.10:87103444:G:A 1089/140182)
Row 194860339 (NC_000005.10:87103444:G:C 114729/140158)

- Apr 26, 2021 (155)
121 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 194860338 (NC_000005.10:87103444:G:A 1089/140182)
Row 194860339 (NC_000005.10:87103444:G:C 114729/140158)

- Apr 26, 2021 (155)
122 Genome of the Netherlands Release 5 NC_000005.9 - 86399262 Apr 26, 2020 (154)
123 HapMap NC_000005.10 - 87103445 Apr 26, 2020 (154)
124 KOREAN population from KRGDB NC_000005.9 - 86399262 Apr 26, 2020 (154)
125 Korean Genome Project NC_000005.10 - 87103445 Apr 26, 2020 (154)
126 Northern Sweden NC_000005.9 - 86399262 Jul 13, 2019 (153)
127 Qatari NC_000005.9 - 86399262 Apr 26, 2020 (154)
128 SGDP_PRJ NC_000005.9 - 86399262 Apr 26, 2020 (154)
129 Siberian NC_000005.9 - 86399262 Apr 26, 2020 (154)
130 8.3KJPN NC_000005.9 - 86399262 Apr 26, 2021 (155)
131 14KJPN NC_000005.10 - 87103445 Oct 13, 2022 (156)
132 TopMed NC_000005.10 - 87103445 Apr 26, 2021 (155)
133 UK 10K study - Twins

Submission ignored due to conflicting rows:
Row 15324856 (NC_000005.9:86399261:G:G 858/3708, NC_000005.9:86399261:G:C 2850/3708)
Row 15324857 (NC_000005.9:86399261:G:G 3708/3708, NC_000005.9:86399261:G:A 0/3708)

- Oct 12, 2018 (152)
134 UK 10K study - Twins

Submission ignored due to conflicting rows:
Row 15324856 (NC_000005.9:86399261:G:G 858/3708, NC_000005.9:86399261:G:C 2850/3708)
Row 15324857 (NC_000005.9:86399261:G:G 3708/3708, NC_000005.9:86399261:G:A 0/3708)

- Oct 12, 2018 (152)
135 A Vietnamese Genetic Variation Database NC_000005.9 - 86399262 Jul 13, 2019 (153)
136 ALFA NC_000005.10 - 87103445 Apr 26, 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)
rs17285892 Oct 08, 2004 (123)
rs57689021 Feb 27, 2009 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
27562405, 16068164, 14323241, ss558524307, ss1315930559, ss1613328408, ss1656322441, ss1803804258, ss2827055518, ss3862306261, ss3908890770, ss5638232417 NC_000005.9:86399261:G:A NC_000005.10:87103444:G:A (self)
36279162, 15097636389, ss2275435510, ss3715090961, ss5264718335, ss5462815144, ss5548753227 NC_000005.10:87103444:G:A NC_000005.10:87103444:G:A (self)
ss66069951, ss75998366, ss93165524, ss109198442, ss112147770, ss116702932, ss165432756, ss166781586, ss170199708, ss200498938, ss206921910, ss253603662, ss278371541, ss285213044, ss293397488, ss480600079, ss1591305276, ss1712779404 NC_000005.8:86435017:G:C NC_000005.10:87103444:G:C (self)
27562405, 10899808, 7388436, 6814934, 16068164, 5824961, 7083699, 14323241, 3801026, 30683043, 3403285, ss221791955, ss233027395, ss240181645, ss480614321, ss481445302, ss485095168, ss537102487, ss558524307, ss652401149, ss779025675, ss782993891, ss783954591, ss832250765, ss834488324, ss981787930, ss1072794668, ss1315930560, ss1430410414, ss1581223497, ss1613328407, ss1656322440, ss1752588419, ss1803804258, ss1925041769, ss1970138559, ss2023128381, ss2151284672, ss2626061078, ss2634304625, ss2706838176, ss2827055518, ss2997280658, ss3346484907, ss3629278874, ss3632230387, ss3633380947, ss3634101786, ss3635010624, ss3635783695, ss3636722735, ss3637536321, ss3640717917, ss3665161560, ss3732540096, ss3745310833, ss3763681997, ss3772804944, ss3785168856, ss3790566099, ss3795442696, ss3829350600, ss3838149594, ss3862306261, ss3908890770, ss5172713736, ss5315066479, ss5638232417, ss5835213758, ss5966667946, ss5980304579 NC_000005.9:86399261:G:C NC_000005.10:87103444:G:C (self)
36279162, 2907568, 13455366, 43221802, 504656809, 15097636389, ss2275435510, ss3025349925, ss3648109473, ss3715090962, ss3806849844, ss3843590909, ss3957077365, ss4667279252, ss5264718334, ss5462815143, ss5548753227, ss5709384698, ss5806502890, ss5854899850 NC_000005.10:87103444:G:C NC_000005.10:87103444:G:C (self)
ss10228035, ss11731065, ss17858407, ss22290239 NT_006713.13:15791393:G:C NC_000005.10:87103444:G:C (self)
ss3568268, ss24621565, ss44637787, ss68941482, ss81815796, ss98631114, ss105935697, ss143268949, ss143579969, ss155705726, ss160557779 NT_006713.15:36993620:G:C NC_000005.10:87103444:G:C (self)
15097636389 NC_000005.10:87103444:G:T NC_000005.10:87103444:G:T (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 rs2544677

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