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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.

rs1700687

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr5:76937179 (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>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.386426 (102283/264690, TOPMED)
T=0.387465 (54073/139556, GnomAD)
T=0.47092 (38171/81056, ALFA) (+ 20 more)
C=0.38131 (10775/28258, 14KJPN)
C=0.38395 (6435/16760, 8.3KJPN)
T=0.4213 (2698/6404, 1000G_30x)
T=0.4291 (2149/5008, 1000G)
C=0.4871 (2182/4480, Estonian)
C=0.4824 (1859/3854, ALSPAC)
C=0.4854 (1800/3708, TWINSUK)
C=0.4788 (1403/2930, KOREAN)
T=0.4409 (918/2082, HGDP_Stanford)
T=0.3707 (697/1880, HapMap)
C=0.4492 (823/1832, Korea1K)
T=0.4780 (543/1136, Daghestan)
C=0.466 (465/998, GoNL)
C=0.497 (298/600, NorthernSweden)
C=0.301 (109/362, SGDP_PRJ)
T=0.347 (75/216, Qatari)
T=0.462 (98/212, Vietnamese)
T=0.16 (12/74, Ancient Sardinia)
C=0.31 (15/48, Siberian)
C=0.47 (19/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
S100Z : 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 81150 C=0.52916 T=0.47084
European Sub 65570 C=0.50732 T=0.49268
African Sub 7164 C=0.8416 T=0.1584
African Others Sub 254 C=0.929 T=0.071
African American Sub 6910 C=0.8384 T=0.1616
Asian Sub 192 C=0.531 T=0.469
East Asian Sub 150 C=0.513 T=0.487
Other Asian Sub 42 C=0.60 T=0.40
Latin American 1 Sub 254 C=0.579 T=0.421
Latin American 2 Sub 1232 C=0.4326 T=0.5674
South Asian Sub 4920 C=0.3768 T=0.6232
Other Sub 1818 C=0.5561 T=0.4439


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 C=0.613574 T=0.386426
gnomAD - Genomes Global Study-wide 139556 C=0.612535 T=0.387465
gnomAD - Genomes European Sub 75634 C=0.50879 T=0.49121
gnomAD - Genomes African Sub 41796 C=0.84085 T=0.15915
gnomAD - Genomes American Sub 13550 C=0.50642 T=0.49358
gnomAD - Genomes Ashkenazi Jewish Sub 3318 C=0.6516 T=0.3484
gnomAD - Genomes East Asian Sub 3110 C=0.4907 T=0.5093
gnomAD - Genomes Other Sub 2148 C=0.6085 T=0.3915
Allele Frequency Aggregator Total Global 81056 C=0.52908 T=0.47092
Allele Frequency Aggregator European Sub 65494 C=0.50724 T=0.49276
Allele Frequency Aggregator African Sub 7164 C=0.8416 T=0.1584
Allele Frequency Aggregator South Asian Sub 4920 C=0.3768 T=0.6232
Allele Frequency Aggregator Other Sub 1800 C=0.5550 T=0.4450
Allele Frequency Aggregator Latin American 2 Sub 1232 C=0.4326 T=0.5674
Allele Frequency Aggregator Latin American 1 Sub 254 C=0.579 T=0.421
Allele Frequency Aggregator Asian Sub 192 C=0.531 T=0.469
14KJPN JAPANESE Study-wide 28258 C=0.38131 T=0.61869
8.3KJPN JAPANESE Study-wide 16760 C=0.38395 T=0.61605
1000Genomes_30x Global Study-wide 6404 C=0.5787 T=0.4213
1000Genomes_30x African Sub 1786 C=0.9082 T=0.0918
1000Genomes_30x Europe Sub 1266 C=0.5427 T=0.4573
1000Genomes_30x South Asian Sub 1202 C=0.2987 T=0.7013
1000Genomes_30x East Asian Sub 1170 C=0.4974 T=0.5026
1000Genomes_30x American Sub 980 C=0.465 T=0.535
1000Genomes Global Study-wide 5008 C=0.5709 T=0.4291
1000Genomes African Sub 1322 C=0.8994 T=0.1006
1000Genomes East Asian Sub 1008 C=0.4960 T=0.5040
1000Genomes Europe Sub 1006 C=0.5368 T=0.4632
1000Genomes South Asian Sub 978 C=0.308 T=0.692
1000Genomes American Sub 694 C=0.474 T=0.526
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.4871 T=0.5129
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.4824 T=0.5176
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.4854 T=0.5146
KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.4788 T=0.5212
HGDP-CEPH-db Supplement 1 Global Study-wide 2082 C=0.5591 T=0.4409
HGDP-CEPH-db Supplement 1 Est_Asia Sub 468 C=0.429 T=0.571
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 C=0.476 T=0.524
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 C=0.771 T=0.229
HGDP-CEPH-db Supplement 1 Europe Sub 320 C=0.588 T=0.412
HGDP-CEPH-db Supplement 1 Africa Sub 242 C=0.913 T=0.087
HGDP-CEPH-db Supplement 1 America Sub 216 C=0.139 T=0.861
HGDP-CEPH-db Supplement 1 Oceania Sub 72 C=0.79 T=0.21
HapMap Global Study-wide 1880 C=0.6293 T=0.3707
HapMap American Sub 770 C=0.487 T=0.513
HapMap African Sub 688 C=0.885 T=0.115
HapMap Asian Sub 248 C=0.435 T=0.565
HapMap Europe Sub 174 C=0.523 T=0.477
Korean Genome Project KOREAN Study-wide 1832 C=0.4492 T=0.5508
Genome-wide autozygosity in Daghestan Global Study-wide 1136 C=0.5220 T=0.4780
Genome-wide autozygosity in Daghestan Daghestan Sub 628 C=0.540 T=0.460
Genome-wide autozygosity in Daghestan Near_East Sub 144 C=0.653 T=0.347
Genome-wide autozygosity in Daghestan Central Asia Sub 122 C=0.459 T=0.541
Genome-wide autozygosity in Daghestan Europe Sub 108 C=0.454 T=0.546
Genome-wide autozygosity in Daghestan South Asian Sub 98 C=0.27 T=0.73
Genome-wide autozygosity in Daghestan Caucasus Sub 36 C=0.81 T=0.19
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.466 T=0.534
Northern Sweden ACPOP Study-wide 600 C=0.497 T=0.503
SGDP_PRJ Global Study-wide 362 C=0.301 T=0.699
Qatari Global Study-wide 216 C=0.653 T=0.347
A Vietnamese Genetic Variation Database Global Study-wide 212 C=0.538 T=0.462
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 74 C=0.84 T=0.16
Siberian Global Study-wide 48 C=0.31 T=0.69
The Danish reference pan genome Danish Study-wide 40 C=0.47 T=0.53
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.76937179C>T
GRCh37.p13 chr 5 NC_000005.9:g.76233004C>T
Gene: S100Z, S100 calcium binding protein Z (plus strand)
Molecule type Change Amino acid[Codon] SO Term
S100Z transcript NM_130772.4:c. N/A Genic Downstream Transcript Variant
S100Z transcript variant X7 XM_011543241.3:c.*3-15656…

XM_011543241.3:c.*3-15656C>T

N/A Intron Variant
S100Z transcript variant X2 XM_011543240.4:c. N/A Genic Downstream Transcript Variant
S100Z transcript variant X8 XM_011543244.3:c. N/A Genic Downstream Transcript Variant
S100Z transcript variant X4 XM_011543245.3:c. N/A Genic Downstream Transcript Variant
S100Z transcript variant X9 XM_017009171.2:c. N/A Genic Downstream Transcript Variant
S100Z transcript variant X1 XM_047416869.1:c. N/A Genic Downstream Transcript Variant
S100Z transcript variant X3 XM_047416871.1:c. N/A Genic Downstream Transcript Variant
S100Z transcript variant X5 XM_047416872.1:c. N/A Genic Downstream Transcript Variant
S100Z transcript variant X6 XM_047416873.1:c. N/A Genic Downstream 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.

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 C= T
GRCh38.p14 chr 5 NC_000005.10:g.76937179= NC_000005.10:g.76937179C>T
GRCh37.p13 chr 5 NC_000005.9:g.76233004= NC_000005.9:g.76233004C>T
S100Z transcript variant X7 XM_011543241.3:c.*3-15656= XM_011543241.3:c.*3-15656C>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#.

96 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss2533934 Nov 09, 2000 (89)
2 SC_JCM ss3785391 Sep 28, 2001 (100)
3 CSHL-HAPMAP ss17089871 Feb 27, 2004 (120)
4 SSAHASNP ss22319833 Apr 05, 2004 (121)
5 PERLEGEN ss24676299 Sep 20, 2004 (123)
6 ABI ss44634165 Mar 13, 2006 (126)
7 ILLUMINA ss67166075 Nov 30, 2006 (127)
8 ILLUMINA ss67518595 Nov 30, 2006 (127)
9 ILLUMINA ss68169289 Dec 12, 2006 (127)
10 PERLEGEN ss68939287 May 17, 2007 (127)
11 ILLUMINA ss70649087 May 25, 2008 (130)
12 ILLUMINA ss71205377 May 17, 2007 (127)
13 ILLUMINA ss75465409 Dec 07, 2007 (129)
14 KRIBB_YJKIM ss83863003 Dec 15, 2007 (130)
15 HUMANGENOME_JCVI ss98626298 Feb 05, 2009 (130)
16 BGI ss105931931 Feb 05, 2009 (130)
17 1000GENOMES ss109141832 Jan 23, 2009 (130)
18 ILLUMINA-UK ss116675440 Feb 14, 2009 (130)
19 ENSEMBL ss143076970 Dec 01, 2009 (131)
20 ILLUMINA ss153596367 Dec 01, 2009 (131)
21 GMI ss155616627 Dec 01, 2009 (131)
22 ILLUMINA ss159302353 Dec 01, 2009 (131)
23 ILLUMINA ss172702433 Jul 04, 2010 (132)
24 1000GENOMES ss221753918 Jul 14, 2010 (132)
25 1000GENOMES ss232999676 Jul 14, 2010 (132)
26 1000GENOMES ss240160297 Jul 15, 2010 (132)
27 GMI ss278344282 May 04, 2012 (137)
28 GMI ss285200209 Apr 25, 2013 (138)
29 PJP ss293383812 May 09, 2011 (134)
30 ILLUMINA ss536932123 Sep 08, 2015 (146)
31 TISHKOFF ss558480312 Apr 25, 2013 (138)
32 SSMP ss652351718 Apr 25, 2013 (138)
33 ILLUMINA ss832814434 Jul 13, 2019 (153)
34 EVA-GONL ss981712399 Aug 21, 2014 (142)
35 JMKIDD_LAB ss1072738899 Aug 21, 2014 (142)
36 1000GENOMES ss1315655012 Aug 21, 2014 (142)
37 HAMMER_LAB ss1397417035 Sep 08, 2015 (146)
38 DDI ss1430386792 Apr 01, 2015 (144)
39 EVA_GENOME_DK ss1581194401 Apr 01, 2015 (144)
40 EVA_DECODE ss1591231896 Apr 01, 2015 (144)
41 EVA_UK10K_ALSPAC ss1613183701 Apr 01, 2015 (144)
42 EVA_UK10K_TWINSUK ss1656177734 Apr 01, 2015 (144)
43 EVA_SVP ss1712774401 Apr 01, 2015 (144)
44 HAMMER_LAB ss1803704263 Sep 08, 2015 (146)
45 WEILL_CORNELL_DGM ss1924969089 Feb 12, 2016 (147)
46 GENOMED ss1970120473 Jul 19, 2016 (147)
47 JJLAB ss2023090433 Sep 14, 2016 (149)
48 USC_VALOUEV ss2151245556 Dec 20, 2016 (150)
49 HUMAN_LONGEVITY ss2274853219 Dec 20, 2016 (150)
50 SYSTEMSBIOZJU ss2626041782 Nov 08, 2017 (151)
51 ILLUMINA ss2635145789 Nov 08, 2017 (151)
52 GRF ss2706795332 Nov 08, 2017 (151)
53 GNOMAD ss2826247212 Nov 08, 2017 (151)
54 AFFY ss2985324480 Nov 08, 2017 (151)
55 AFFY ss2985955251 Nov 08, 2017 (151)
56 SWEGEN ss2997164631 Nov 08, 2017 (151)
57 BIOINF_KMB_FNS_UNIBA ss3025329680 Nov 08, 2017 (151)
58 CSHL ss3346451367 Nov 08, 2017 (151)
59 ILLUMINA ss3629264020 Oct 12, 2018 (152)
60 ILLUMINA ss3638561179 Oct 12, 2018 (152)
61 ILLUMINA ss3639283221 Oct 12, 2018 (152)
62 ILLUMINA ss3639939037 Oct 12, 2018 (152)
63 ILLUMINA ss3643506643 Oct 12, 2018 (152)
64 ILLUMINA ss3643984548 Oct 12, 2018 (152)
65 URBANLAB ss3648093228 Oct 12, 2018 (152)
66 ILLUMINA ss3654098253 Oct 12, 2018 (152)
67 EGCUT_WGS ss3665043267 Jul 13, 2019 (153)
68 EVA_DECODE ss3714954108 Jul 13, 2019 (153)
69 ACPOP ss3732476994 Jul 13, 2019 (153)
70 EVA ss3763598367 Jul 13, 2019 (153)
71 PACBIO ss3785148799 Jul 13, 2019 (153)
72 PACBIO ss3790548992 Jul 13, 2019 (153)
73 PACBIO ss3795425576 Jul 13, 2019 (153)
74 KHV_HUMAN_GENOMES ss3806766144 Jul 13, 2019 (153)
75 EVA ss3829313694 Apr 26, 2020 (154)
76 EVA ss3838130139 Apr 26, 2020 (154)
77 EVA ss3843571007 Apr 26, 2020 (154)
78 HGDP ss3847795115 Apr 26, 2020 (154)
79 SGDP_PRJ ss3862157941 Apr 26, 2020 (154)
80 KRGDB ss3908726392 Apr 26, 2020 (154)
81 KOGIC ss3956943867 Apr 26, 2020 (154)
82 EVA ss3985149362 Apr 26, 2021 (155)
83 EVA ss4017213714 Apr 26, 2021 (155)
84 TOPMED ss4664853908 Apr 26, 2021 (155)
85 TOMMO_GENOMICS ss5172391848 Apr 26, 2021 (155)
86 1000G_HIGH_COVERAGE ss5264470010 Oct 17, 2022 (156)
87 EVA ss5358467990 Oct 17, 2022 (156)
88 HUGCELL_USP ss5462592247 Oct 17, 2022 (156)
89 1000G_HIGH_COVERAGE ss5548376253 Oct 17, 2022 (156)
90 SANFORD_IMAGENETICS ss5638088681 Oct 17, 2022 (156)
91 TOMMO_GENOMICS ss5708973652 Oct 17, 2022 (156)
92 YY_MCH ss5806441542 Oct 17, 2022 (156)
93 EVA ss5835117511 Oct 17, 2022 (156)
94 EVA ss5854869770 Oct 17, 2022 (156)
95 EVA ss5894745038 Oct 17, 2022 (156)
96 EVA ss5966519845 Oct 17, 2022 (156)
97 1000Genomes NC_000005.9 - 76233004 Oct 12, 2018 (152)
98 1000Genomes_30x NC_000005.10 - 76937179 Oct 17, 2022 (156)
99 The Avon Longitudinal Study of Parents and Children NC_000005.9 - 76233004 Oct 12, 2018 (152)
100 Genome-wide autozygosity in Daghestan NC_000005.8 - 76268760 Apr 26, 2020 (154)
101 Genetic variation in the Estonian population NC_000005.9 - 76233004 Oct 12, 2018 (152)
102 The Danish reference pan genome NC_000005.9 - 76233004 Apr 26, 2020 (154)
103 gnomAD - Genomes NC_000005.10 - 76937179 Apr 26, 2021 (155)
104 Genome of the Netherlands Release 5 NC_000005.9 - 76233004 Apr 26, 2020 (154)
105 HGDP-CEPH-db Supplement 1 NC_000005.8 - 76268760 Apr 26, 2020 (154)
106 HapMap NC_000005.10 - 76937179 Apr 26, 2020 (154)
107 KOREAN population from KRGDB NC_000005.9 - 76233004 Apr 26, 2020 (154)
108 Korean Genome Project NC_000005.10 - 76937179 Apr 26, 2020 (154)
109 Northern Sweden NC_000005.9 - 76233004 Jul 13, 2019 (153)
110 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000005.9 - 76233004 Apr 26, 2021 (155)
111 Qatari NC_000005.9 - 76233004 Apr 26, 2020 (154)
112 SGDP_PRJ NC_000005.9 - 76233004 Apr 26, 2020 (154)
113 Siberian NC_000005.9 - 76233004 Apr 26, 2020 (154)
114 8.3KJPN NC_000005.9 - 76233004 Apr 26, 2021 (155)
115 14KJPN NC_000005.10 - 76937179 Oct 17, 2022 (156)
116 TopMed NC_000005.10 - 76937179 Apr 26, 2021 (155)
117 UK 10K study - Twins NC_000005.9 - 76233004 Oct 12, 2018 (152)
118 A Vietnamese Genetic Variation Database NC_000005.9 - 76233004 Jul 13, 2019 (153)
119 ALFA NC_000005.10 - 76937179 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)
rs17670152 Oct 08, 2004 (123)
rs59399151 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
392027, 473007, ss109141832, ss116675440, ss278344282, ss285200209, ss293383812, ss1397417035, ss1591231896, ss1712774401, ss2635145789, ss3639283221, ss3639939037, ss3643506643, ss3643984548, ss3847795115 NC_000005.8:76268759:C:T NC_000005.10:76937178:C:T (self)
27275461, 15164697, 10781515, 7359340, 6741686, 15903786, 5761859, 375289, 7011019, 14174921, 3761910, 30361155, 15164697, 3366555, ss221753918, ss232999676, ss240160297, ss536932123, ss558480312, ss652351718, ss832814434, ss981712399, ss1072738899, ss1315655012, ss1430386792, ss1581194401, ss1613183701, ss1656177734, ss1803704263, ss1924969089, ss1970120473, ss2023090433, ss2151245556, ss2626041782, ss2706795332, ss2826247212, ss2985324480, ss2985955251, ss2997164631, ss3346451367, ss3629264020, ss3638561179, ss3654098253, ss3665043267, ss3732476994, ss3763598367, ss3785148799, ss3790548992, ss3795425576, ss3829313694, ss3838130139, ss3862157941, ss3908726392, ss3985149362, ss4017213714, ss5172391848, ss5358467990, ss5638088681, ss5835117511, ss5966519845 NC_000005.9:76233003:C:T NC_000005.10:76937178:C:T (self)
35902188, 192799524, 2894182, 13321868, 42810756, 502231465, 5329092539, ss2274853219, ss3025329680, ss3648093228, ss3714954108, ss3806766144, ss3843571007, ss3956943867, ss4664853908, ss5264470010, ss5462592247, ss5548376253, ss5708973652, ss5806441542, ss5854869770, ss5894745038 NC_000005.10:76937178:C:T NC_000005.10:76937178:C:T (self)
ss17089871, ss22319833 NT_006713.13:5625135:C:T NC_000005.10:76937178:C:T (self)
ss2533934, ss3785391, ss24676299, ss44634165, ss67166075, ss67518595, ss68169289, ss68939287, ss70649087, ss71205377, ss75465409, ss83863003, ss98626298, ss105931931, ss143076970, ss153596367, ss155616627, ss159302353, ss172702433 NT_006713.15:26827362:C:T NC_000005.10:76937178:C: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 rs1700687

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