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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.

rs169

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr7:25006722 (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
A>G
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.143341 (37941/264690, TOPMED)
A=0.182204 (36424/199908, ALFA)
A=0.153130 (21452/140090, GnomAD) (+ 19 more)
A=0.23123 (6534/28258, 14KJPN)
A=0.23004 (3855/16758, 8.3KJPN)
A=0.1179 (755/6404, 1000G_30x)
A=0.1224 (613/5008, 1000G)
A=0.1815 (813/4480, Estonian)
A=0.2161 (833/3854, ALSPAC)
A=0.1998 (741/3708, TWINSUK)
A=0.1829 (536/2930, KOREAN)
A=0.0989 (206/2082, HGDP_Stanford)
A=0.1071 (202/1886, HapMap)
A=0.1894 (347/1832, Korea1K)
A=0.223 (223/998, GoNL)
A=0.212 (127/600, NorthernSweden)
A=0.089 (48/542, SGDP_PRJ)
A=0.097 (21/216, Qatari)
A=0.131 (28/214, Vietnamese)
A=0.24 (22/92, Ancient Sardinia)
A=0.13 (7/54, Siberian)
A=0.33 (13/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
Publications
1 citation
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 199908 A=0.182204 G=0.817796
European Sub 172688 A=0.193140 G=0.806860
African Sub 7092 A=0.0642 G=0.9358
African Others Sub 264 A=0.038 G=0.962
African American Sub 6828 A=0.0652 G=0.9348
Asian Sub 702 A=0.152 G=0.848
East Asian Sub 556 A=0.164 G=0.836
Other Asian Sub 146 A=0.110 G=0.890
Latin American 1 Sub 844 A=0.108 G=0.892
Latin American 2 Sub 6902 A=0.1375 G=0.8625
South Asian Sub 5036 A=0.0755 G=0.9245
Other Sub 6644 A=0.1639 G=0.8361


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 A=0.143341 G=0.856659
Allele Frequency Aggregator Total Global 199908 A=0.182204 G=0.817796
Allele Frequency Aggregator European Sub 172688 A=0.193140 G=0.806860
Allele Frequency Aggregator African Sub 7092 A=0.0642 G=0.9358
Allele Frequency Aggregator Latin American 2 Sub 6902 A=0.1375 G=0.8625
Allele Frequency Aggregator Other Sub 6644 A=0.1639 G=0.8361
Allele Frequency Aggregator South Asian Sub 5036 A=0.0755 G=0.9245
Allele Frequency Aggregator Latin American 1 Sub 844 A=0.108 G=0.892
Allele Frequency Aggregator Asian Sub 702 A=0.152 G=0.848
gnomAD - Genomes Global Study-wide 140090 A=0.153130 G=0.846870
gnomAD - Genomes European Sub 75858 A=0.20425 G=0.79575
gnomAD - Genomes African Sub 41986 A=0.06519 G=0.93481
gnomAD - Genomes American Sub 13644 A=0.12980 G=0.87020
gnomAD - Genomes Ashkenazi Jewish Sub 3324 A=0.1971 G=0.8029
gnomAD - Genomes East Asian Sub 3126 A=0.1542 G=0.8458
gnomAD - Genomes Other Sub 2152 A=0.1454 G=0.8546
14KJPN JAPANESE Study-wide 28258 A=0.23123 G=0.76877
8.3KJPN JAPANESE Study-wide 16758 A=0.23004 G=0.76996
1000Genomes_30x Global Study-wide 6404 A=0.1179 G=0.8821
1000Genomes_30x African Sub 1786 A=0.0420 G=0.9580
1000Genomes_30x Europe Sub 1266 A=0.2164 G=0.7836
1000Genomes_30x South Asian Sub 1202 A=0.0532 G=0.9468
1000Genomes_30x East Asian Sub 1170 A=0.1778 G=0.8222
1000Genomes_30x American Sub 980 A=0.137 G=0.863
1000Genomes Global Study-wide 5008 A=0.1224 G=0.8776
1000Genomes African Sub 1322 A=0.0461 G=0.9539
1000Genomes East Asian Sub 1008 A=0.1746 G=0.8254
1000Genomes Europe Sub 1006 A=0.2187 G=0.7813
1000Genomes South Asian Sub 978 A=0.057 G=0.943
1000Genomes American Sub 694 A=0.144 G=0.856
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.1815 G=0.8185
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.2161 G=0.7839
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.1998 G=0.8002
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.1829 G=0.8171
HGDP-CEPH-db Supplement 1 Global Study-wide 2082 A=0.0989 G=0.9011
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 A=0.149 G=0.851
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.085 G=0.915
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.080 G=0.920
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.184 G=0.816
HGDP-CEPH-db Supplement 1 Africa Sub 242 A=0.021 G=0.979
HGDP-CEPH-db Supplement 1 America Sub 214 A=0.042 G=0.958
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.00 G=1.00
HapMap Global Study-wide 1886 A=0.1071 G=0.8929
HapMap American Sub 766 A=0.119 G=0.881
HapMap African Sub 692 A=0.039 G=0.961
HapMap Asian Sub 252 A=0.194 G=0.806
HapMap Europe Sub 176 A=0.199 G=0.801
Korean Genome Project KOREAN Study-wide 1832 A=0.1894 G=0.8106
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.223 G=0.777
Northern Sweden ACPOP Study-wide 600 A=0.212 G=0.788
SGDP_PRJ Global Study-wide 542 A=0.089 G=0.911
Qatari Global Study-wide 216 A=0.097 G=0.903
A Vietnamese Genetic Variation Database Global Study-wide 214 A=0.131 G=0.869
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 92 A=0.24 G=0.76
Siberian Global Study-wide 54 A=0.13 G=0.87
The Danish reference pan genome Danish Study-wide 40 A=0.33 G=0.68
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 7 NC_000007.14:g.25006722A>G
GRCh37.p13 chr 7 NC_000007.13:g.25046341A>G
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 A= G
GRCh38.p14 chr 7 NC_000007.14:g.25006722= NC_000007.14:g.25006722A>G
GRCh37.p13 chr 7 NC_000007.13:g.25046341= NC_000007.13:g.25046341A>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#.

125 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 KWOK ss169 Sep 19, 2000 (36)
2 SC_JCM ss3535315 Sep 28, 2001 (120)
3 SC_SNP ss14763478 Dec 05, 2003 (120)
4 ABI ss43052162 Mar 13, 2006 (126)
5 ILLUMINA ss67156343 Dec 02, 2006 (127)
6 ILLUMINA ss67501220 Dec 02, 2006 (127)
7 ILLUMINA ss68164642 Dec 12, 2006 (127)
8 ILLUMINA ss70643539 May 25, 2008 (130)
9 ILLUMINA ss71196740 May 18, 2007 (127)
10 ILLUMINA ss75801935 Dec 06, 2007 (129)
11 HGSV ss78917551 Dec 06, 2007 (129)
12 KRIBB_YJKIM ss83344007 Dec 15, 2007 (130)
13 HGSV ss85219358 Dec 15, 2007 (130)
14 HGSV ss85390925 Dec 15, 2007 (130)
15 BCMHGSC_JDW ss93646359 Mar 24, 2008 (129)
16 HUMANGENOME_JCVI ss98139999 Feb 05, 2009 (130)
17 BGI ss105507404 Feb 05, 2009 (130)
18 1000GENOMES ss111692217 Jan 25, 2009 (130)
19 1000GENOMES ss113478663 Jan 25, 2009 (130)
20 ILLUMINA-UK ss115987924 Feb 14, 2009 (130)
21 ENSEMBL ss142694584 Dec 01, 2009 (131)
22 ENSEMBL ss142761021 Dec 01, 2009 (131)
23 ILLUMINA ss153572179 Dec 01, 2009 (131)
24 GMI ss154529585 Dec 01, 2009 (131)
25 ILLUMINA ss159296482 Dec 01, 2009 (131)
26 ILLUMINA ss160394231 Dec 01, 2009 (131)
27 COMPLETE_GENOMICS ss162142063 Jul 04, 2010 (132)
28 COMPLETE_GENOMICS ss163848854 Jul 04, 2010 (132)
29 COMPLETE_GENOMICS ss166295802 Jul 04, 2010 (132)
30 ILLUMINA ss172652317 Jul 04, 2010 (132)
31 BUSHMAN ss203090239 Jul 04, 2010 (132)
32 BCM-HGSC-SUB ss208087363 Jul 04, 2010 (132)
33 1000GENOMES ss222968962 Jul 14, 2010 (132)
34 1000GENOMES ss233894698 Jul 15, 2010 (132)
35 1000GENOMES ss240866163 Jul 15, 2010 (132)
36 BL ss254128471 May 09, 2011 (134)
37 GMI ss279229324 May 04, 2012 (137)
38 GMI ss285592485 Apr 25, 2013 (138)
39 PJP ss294032376 May 09, 2011 (134)
40 ILLUMINA ss480096568 May 04, 2012 (137)
41 ILLUMINA ss480105424 May 04, 2012 (137)
42 ILLUMINA ss480793869 Sep 08, 2015 (146)
43 ILLUMINA ss484846140 May 04, 2012 (137)
44 ILLUMINA ss536916743 Sep 08, 2015 (146)
45 TISHKOFF ss559876073 Apr 25, 2013 (138)
46 SSMP ss654229455 Apr 25, 2013 (138)
47 ILLUMINA ss778445515 Aug 21, 2014 (142)
48 ILLUMINA ss782869609 Aug 21, 2014 (142)
49 ILLUMINA ss783833714 Aug 21, 2014 (142)
50 ILLUMINA ss832123759 Apr 01, 2015 (144)
51 ILLUMINA ss832808577 Aug 21, 2014 (142)
52 ILLUMINA ss833399407 Aug 21, 2014 (142)
53 ILLUMINA ss833901081 Aug 21, 2014 (142)
54 EVA-GONL ss984064770 Aug 21, 2014 (142)
55 JMKIDD_LAB ss1074451799 Aug 21, 2014 (142)
56 1000GENOMES ss1324348538 Aug 21, 2014 (142)
57 DDI ss1431061427 Apr 01, 2015 (144)
58 EVA_GENOME_DK ss1582116940 Apr 01, 2015 (144)
59 EVA_DECODE ss1593633668 Apr 01, 2015 (144)
60 EVA_UK10K_ALSPAC ss1617795554 Apr 01, 2015 (144)
61 EVA_UK10K_TWINSUK ss1660789587 Apr 01, 2015 (144)
62 EVA_SVP ss1712939995 Apr 01, 2015 (144)
63 ILLUMINA ss1752679507 Sep 08, 2015 (146)
64 HAMMER_LAB ss1804917068 Sep 08, 2015 (146)
65 WEILL_CORNELL_DGM ss1927309749 Feb 12, 2016 (147)
66 GENOMED ss1970651750 Jul 19, 2016 (147)
67 JJLAB ss2024332087 Sep 14, 2016 (149)
68 USC_VALOUEV ss2152528147 Dec 20, 2016 (150)
69 HUMAN_LONGEVITY ss2292531139 Dec 20, 2016 (150)
70 SYSTEMSBIOZJU ss2626654944 Nov 08, 2017 (151)
71 ILLUMINA ss2634581370 Nov 08, 2017 (151)
72 GRF ss2708184973 Nov 08, 2017 (151)
73 GNOMAD ss2850936074 Nov 08, 2017 (151)
74 SWEGEN ss3000795131 Nov 08, 2017 (151)
75 BIOINF_KMB_FNS_UNIBA ss3025960299 Nov 08, 2017 (151)
76 CSHL ss3347488553 Nov 08, 2017 (151)
77 ILLUMINA ss3629774631 Oct 12, 2018 (152)
78 ILLUMINA ss3632490145 Oct 12, 2018 (152)
79 ILLUMINA ss3633456482 Oct 12, 2018 (152)
80 ILLUMINA ss3634181076 Oct 12, 2018 (152)
81 ILLUMINA ss3635112883 Oct 12, 2018 (152)
82 ILLUMINA ss3635861051 Oct 12, 2018 (152)
83 ILLUMINA ss3636843467 Oct 12, 2018 (152)
84 ILLUMINA ss3637613996 Oct 12, 2018 (152)
85 ILLUMINA ss3638686458 Oct 12, 2018 (152)
86 ILLUMINA ss3639345663 Oct 12, 2018 (152)
87 ILLUMINA ss3639967742 Oct 12, 2018 (152)
88 ILLUMINA ss3640820179 Oct 12, 2018 (152)
89 ILLUMINA ss3643623424 Oct 12, 2018 (152)
90 ILLUMINA ss3644012001 Oct 12, 2018 (152)
91 URBANLAB ss3648585954 Oct 12, 2018 (152)
92 EGCUT_WGS ss3668723959 Jul 13, 2019 (153)
93 EVA_DECODE ss3719305672 Jul 13, 2019 (153)
94 ACPOP ss3734452431 Jul 13, 2019 (153)
95 ILLUMINA ss3745412767 Jul 13, 2019 (153)
96 EVA ss3766317532 Jul 13, 2019 (153)
97 ILLUMINA ss3772905948 Jul 13, 2019 (153)
98 PACBIO ss3785760901 Jul 13, 2019 (153)
99 PACBIO ss3791071320 Jul 13, 2019 (153)
100 PACBIO ss3795951076 Jul 13, 2019 (153)
101 KHV_HUMAN_GENOMES ss3809484983 Jul 13, 2019 (153)
102 EVA ss3830470867 Apr 26, 2020 (154)
103 EVA ss3838722716 Apr 26, 2020 (154)
104 EVA ss3844173976 Apr 26, 2020 (154)
105 HGDP ss3847870022 Apr 26, 2020 (154)
106 SGDP_PRJ ss3866854539 Apr 26, 2020 (154)
107 KRGDB ss3913892707 Apr 26, 2020 (154)
108 KOGIC ss3961078746 Apr 26, 2020 (154)
109 EVA ss3985283893 Apr 26, 2021 (155)
110 EVA ss4017326153 Apr 26, 2021 (155)
111 TOPMED ss4739200976 Apr 26, 2021 (155)
112 TOMMO_GENOMICS ss5182272102 Apr 26, 2021 (155)
113 1000G_HIGH_COVERAGE ss5272194631 Oct 14, 2022 (156)
114 EVA ss5315233319 Oct 14, 2022 (156)
115 EVA ss5372311251 Oct 14, 2022 (156)
116 HUGCELL_USP ss5469443020 Oct 14, 2022 (156)
117 EVA ss5508885968 Oct 14, 2022 (156)
118 1000G_HIGH_COVERAGE ss5560020876 Oct 14, 2022 (156)
119 SANFORD_IMAGENETICS ss5642557659 Oct 14, 2022 (156)
120 TOMMO_GENOMICS ss5721855096 Oct 14, 2022 (156)
121 YY_MCH ss5808428136 Oct 14, 2022 (156)
122 EVA ss5822551989 Oct 14, 2022 (156)
123 EVA ss5855809659 Oct 14, 2022 (156)
124 EVA ss5858125970 Oct 14, 2022 (156)
125 EVA ss5971758303 Oct 14, 2022 (156)
126 1000Genomes NC_000007.13 - 25046341 Oct 12, 2018 (152)
127 1000Genomes_30x NC_000007.14 - 25006722 Oct 14, 2022 (156)
128 The Avon Longitudinal Study of Parents and Children NC_000007.13 - 25046341 Oct 12, 2018 (152)
129 Genetic variation in the Estonian population NC_000007.13 - 25046341 Oct 12, 2018 (152)
130 The Danish reference pan genome NC_000007.13 - 25046341 Apr 26, 2020 (154)
131 gnomAD - Genomes NC_000007.14 - 25006722 Apr 26, 2021 (155)
132 Genome of the Netherlands Release 5 NC_000007.13 - 25046341 Apr 26, 2020 (154)
133 HGDP-CEPH-db Supplement 1 NC_000007.12 - 25012866 Apr 26, 2020 (154)
134 HapMap NC_000007.14 - 25006722 Apr 26, 2020 (154)
135 KOREAN population from KRGDB NC_000007.13 - 25046341 Apr 26, 2020 (154)
136 Korean Genome Project NC_000007.14 - 25006722 Apr 26, 2020 (154)
137 Northern Sweden NC_000007.13 - 25046341 Jul 13, 2019 (153)
138 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000007.13 - 25046341 Apr 26, 2021 (155)
139 Qatari NC_000007.13 - 25046341 Apr 26, 2020 (154)
140 SGDP_PRJ NC_000007.13 - 25046341 Apr 26, 2020 (154)
141 Siberian NC_000007.13 - 25046341 Apr 26, 2020 (154)
142 8.3KJPN NC_000007.13 - 25046341 Apr 26, 2021 (155)
143 14KJPN NC_000007.14 - 25006722 Oct 14, 2022 (156)
144 TopMed NC_000007.14 - 25006722 Apr 26, 2021 (155)
145 UK 10K study - Twins NC_000007.13 - 25046341 Oct 12, 2018 (152)
146 A Vietnamese Genetic Variation Database NC_000007.13 - 25046341 Jul 13, 2019 (153)
147 ALFA NC_000007.14 - 25006722 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)
rs2522225 Feb 27, 2004 (120)
rs10441070 Feb 27, 2004 (120)
rs59828371 May 25, 2008 (130)
rs118194984 Apr 25, 2013 (138)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss78917551, ss85219358, ss85390925, ss3639345663, ss3639967742, ss3644012001 NC_000007.11:24819580:A:G NC_000007.14:25006721:A:G (self)
547914, ss93646359, ss111692217, ss113478663, ss115987924, ss160394231, ss162142063, ss163848854, ss166295802, ss203090239, ss208087363, ss254128471, ss279229324, ss285592485, ss294032376, ss480096568, ss1593633668, ss1712939995, ss3643623424, ss3847870022 NC_000007.12:25012865:A:G NC_000007.14:25006721:A:G (self)
36290580, 20231593, 14462207, 8281879, 9020402, 21070101, 7737296, 509820, 9351679, 18871519, 5044501, 40241409, 20231593, 4507922, ss222968962, ss233894698, ss240866163, ss480105424, ss480793869, ss484846140, ss536916743, ss559876073, ss654229455, ss778445515, ss782869609, ss783833714, ss832123759, ss832808577, ss833399407, ss833901081, ss984064770, ss1074451799, ss1324348538, ss1431061427, ss1582116940, ss1617795554, ss1660789587, ss1752679507, ss1804917068, ss1927309749, ss1970651750, ss2024332087, ss2152528147, ss2626654944, ss2634581370, ss2708184973, ss2850936074, ss3000795131, ss3347488553, ss3629774631, ss3632490145, ss3633456482, ss3634181076, ss3635112883, ss3635861051, ss3636843467, ss3637613996, ss3638686458, ss3640820179, ss3668723959, ss3734452431, ss3745412767, ss3766317532, ss3772905948, ss3785760901, ss3791071320, ss3795951076, ss3830470867, ss3838722716, ss3866854539, ss3913892707, ss3985283893, ss4017326153, ss5182272102, ss5315233319, ss5372311251, ss5508885968, ss5642557659, ss5822551989, ss5971758303 NC_000007.13:25046340:A:G NC_000007.14:25006721:A:G (self)
47546811, 255889547, 3358980, 17456747, 55692200, 576578535, 8058352464, ss2292531139, ss3025960299, ss3648585954, ss3719305672, ss3809484983, ss3844173976, ss3961078746, ss4739200976, ss5272194631, ss5469443020, ss5560020876, ss5721855096, ss5808428136, ss5855809659, ss5858125970 NC_000007.14:25006721:A:G NC_000007.14:25006721:A:G (self)
ss14763478 NT_007819.14:24339948:A:G NC_000007.14:25006721:A:G (self)
ss169, ss3535315, ss43052162, ss67156343, ss67501220, ss68164642, ss70643539, ss71196740, ss75801935, ss83344007, ss98139999, ss105507404, ss142694584, ss142761021, ss153572179, ss154529585, ss159296482, ss172652317 NT_007819.17:25036340:A:G NC_000007.14:25006721:A:G (self)
Help

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

1 citation for rs169
PMID Title Author Year Journal
19440451 Haplotypes in SLC24A5 Gene as Ancestry Informative Markers in Different Populations. Giardina E et al. 2008 Current genomics
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