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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.

rs158805

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr5:74190825 (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=0.264286 (78584/297344, ALFA)
G=0.233137 (61709/264690, TOPMED)
G=0.235140 (32944/140104, GnomAD) (+ 21 more)
G=0.22228 (17477/78626, PAGE_STUDY)
G=0.21714 (6136/28258, 14KJPN)
G=0.21581 (3617/16760, 8.3KJPN)
G=0.2383 (1526/6404, 1000G_30x)
G=0.2410 (1207/5008, 1000G)
G=0.2721 (1219/4480, Estonian)
G=0.2730 (1052/3854, ALSPAC)
G=0.2516 (933/3708, TWINSUK)
G=0.2205 (646/2930, KOREAN)
G=0.2433 (507/2084, HGDP_Stanford)
G=0.2008 (380/1892, HapMap)
G=0.2009 (368/1832, Korea1K)
G=0.271 (270/998, GoNL)
G=0.232 (183/790, PRJEB37584)
G=0.275 (165/600, NorthernSweden)
G=0.180 (93/518, SGDP_PRJ)
G=0.227 (49/216, Qatari)
G=0.255 (54/212, Vietnamese)
G=0.20 (11/54, Siberian)
G=0.23 (10/44, Ancient Sardinia)
G=0.20 (8/40, 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 302472 G=0.263747 A=0.000000, T=0.736253
European Sub 269696 G=0.266215 A=0.000000, T=0.733785
African Sub 6684 G=0.1701 A=0.0000, T=0.8299
African Others Sub 288 G=0.097 A=0.000, T=0.903
African American Sub 6396 G=0.1734 A=0.0000, T=0.8266
Asian Sub 3838 G=0.2285 A=0.0000, T=0.7715
East Asian Sub 3114 G=0.2232 A=0.0000, T=0.7768
Other Asian Sub 724 G=0.251 A=0.000, T=0.749
Latin American 1 Sub 1006 G=0.2674 A=0.0000, T=0.7326
Latin American 2 Sub 6634 G=0.2876 A=0.0000, T=0.7124
South Asian Sub 5136 G=0.2736 A=0.0000, T=0.7264
Other Sub 9478 G=0.2514 A=0.0000, T=0.7486


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
Allele Frequency Aggregator Total Global 297344 G=0.264286 A=0.000000, T=0.735714
Allele Frequency Aggregator European Sub 266526 G=0.266304 A=0.000000, T=0.733696
Allele Frequency Aggregator Other Sub 8660 G=0.2524 A=0.0000, T=0.7476
Allele Frequency Aggregator Latin American 2 Sub 6634 G=0.2876 A=0.0000, T=0.7124
Allele Frequency Aggregator African Sub 5544 G=0.1735 A=0.0000, T=0.8265
Allele Frequency Aggregator South Asian Sub 5136 G=0.2736 A=0.0000, T=0.7264
Allele Frequency Aggregator Asian Sub 3838 G=0.2285 A=0.0000, T=0.7715
Allele Frequency Aggregator Latin American 1 Sub 1006 G=0.2674 A=0.0000, T=0.7326
TopMed Global Study-wide 264690 G=0.233137 T=0.766863
gnomAD - Genomes Global Study-wide 140104 G=0.235140 T=0.764860
gnomAD - Genomes European Sub 75862 G=0.26785 T=0.73215
gnomAD - Genomes African Sub 42012 G=0.16745 T=0.83255
gnomAD - Genomes American Sub 13630 G=0.25525 T=0.74475
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=0.2441 T=0.7559
gnomAD - Genomes East Asian Sub 3130 G=0.2482 T=0.7518
gnomAD - Genomes Other Sub 2148 G=0.2430 T=0.7570
The PAGE Study Global Study-wide 78626 G=0.22228 T=0.77772
The PAGE Study AfricanAmerican Sub 32460 G=0.17264 T=0.82736
The PAGE Study Mexican Sub 10802 G=0.28550 T=0.71450
The PAGE Study Asian Sub 8316 G=0.2174 T=0.7826
The PAGE Study PuertoRican Sub 7916 G=0.2620 T=0.7380
The PAGE Study NativeHawaiian Sub 4534 G=0.2772 T=0.7228
The PAGE Study Cuban Sub 4226 G=0.2657 T=0.7343
The PAGE Study Dominican Sub 3824 G=0.2173 T=0.7827
The PAGE Study CentralAmerican Sub 2450 G=0.2453 T=0.7547
The PAGE Study SouthAmerican Sub 1982 G=0.2745 T=0.7255
The PAGE Study NativeAmerican Sub 1260 G=0.2603 T=0.7397
The PAGE Study SouthAsian Sub 856 G=0.261 T=0.739
14KJPN JAPANESE Study-wide 28258 G=0.21714 T=0.78286
8.3KJPN JAPANESE Study-wide 16760 G=0.21581 T=0.78419
1000Genomes_30x Global Study-wide 6404 G=0.2383 T=0.7617
1000Genomes_30x African Sub 1786 G=0.1562 T=0.8438
1000Genomes_30x Europe Sub 1266 G=0.2559 T=0.7441
1000Genomes_30x South Asian Sub 1202 G=0.2837 T=0.7163
1000Genomes_30x East Asian Sub 1170 G=0.2615 T=0.7385
1000Genomes_30x American Sub 980 G=0.282 T=0.718
1000Genomes Global Study-wide 5008 G=0.2410 T=0.7590
1000Genomes African Sub 1322 G=0.1634 T=0.8366
1000Genomes East Asian Sub 1008 G=0.2659 T=0.7341
1000Genomes Europe Sub 1006 G=0.2604 T=0.7396
1000Genomes South Asian Sub 978 G=0.276 T=0.724
1000Genomes American Sub 694 G=0.275 T=0.725
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.2721 T=0.7279
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.2730 T=0.7270
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.2516 T=0.7484
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.2205 C=0.0000, T=0.7795
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.2433 T=0.7567
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.234 T=0.766
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.266 T=0.734
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.229 T=0.771
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.250 T=0.750
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.107 T=0.893
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.454 T=0.546
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.04 T=0.96
HapMap Global Study-wide 1892 G=0.2008 T=0.7992
HapMap American Sub 770 G=0.238 T=0.762
HapMap African Sub 692 G=0.137 T=0.863
HapMap Asian Sub 254 G=0.228 T=0.772
HapMap Europe Sub 176 G=0.250 T=0.750
Korean Genome Project KOREAN Study-wide 1832 G=0.2009 T=0.7991
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.271 T=0.729
CNV burdens in cranial meningiomas Global Study-wide 790 G=0.232 T=0.768
CNV burdens in cranial meningiomas CRM Sub 790 G=0.232 T=0.768
Northern Sweden ACPOP Study-wide 600 G=0.275 T=0.725
SGDP_PRJ Global Study-wide 518 G=0.180 T=0.820
Qatari Global Study-wide 216 G=0.227 T=0.773
A Vietnamese Genetic Variation Database Global Study-wide 212 G=0.255 T=0.745
Siberian Global Study-wide 54 G=0.20 T=0.80
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 44 G=0.23 T=0.77
The Danish reference pan genome Danish Study-wide 40 G=0.20 T=0.80
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.74190825G>A
GRCh38.p14 chr 5 NC_000005.10:g.74190825G>C
GRCh38.p14 chr 5 NC_000005.10:g.74190825G>T
GRCh37.p13 chr 5 NC_000005.9:g.73486650G>A
GRCh37.p13 chr 5 NC_000005.9:g.73486650G>C
GRCh37.p13 chr 5 NC_000005.9:g.73486650G>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.74190825= NC_000005.10:g.74190825G>A NC_000005.10:g.74190825G>C NC_000005.10:g.74190825G>T
GRCh37.p13 chr 5 NC_000005.9:g.73486650= NC_000005.9:g.73486650G>A NC_000005.9:g.73486650G>C NC_000005.9:g.73486650G>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#.

148 SubSNP, 24 Frequency submissions
No Submitter Submission ID Date (Build)
1 KWOK ss375018 Jul 12, 2000 (79)
2 KWOK ss378225 Jul 12, 2000 (79)
3 SC_JCM ss570307 Jul 16, 2000 (80)
4 KWOK ss1089852 Oct 04, 2000 (86)
5 KWOK ss1091709 Oct 04, 2000 (86)
6 WI_SSAHASNP ss11754226 Jul 11, 2003 (116)
7 SSAHASNP ss22336671 Apr 05, 2004 (121)
8 ABI ss42521131 Mar 14, 2006 (126)
9 ILLUMINA ss66830902 Nov 30, 2006 (127)
10 ILLUMINA ss67139380 Nov 30, 2006 (127)
11 ILLUMINA ss67480062 Nov 30, 2006 (127)
12 PERLEGEN ss68938576 May 17, 2007 (127)
13 ILLUMINA ss70445364 May 17, 2007 (127)
14 ILLUMINA ss70635642 May 25, 2008 (130)
15 ILLUMINA ss71186199 May 17, 2007 (127)
16 AFFY ss74844985 Aug 16, 2007 (128)
17 ILLUMINA ss75879871 Dec 07, 2007 (129)
18 HGSV ss78035046 Dec 07, 2007 (129)
19 KRIBB_YJKIM ss83371241 Dec 15, 2007 (130)
20 BCMHGSC_JDW ss93136862 Mar 24, 2008 (129)
21 HUMANGENOME_JCVI ss98734521 Feb 05, 2009 (130)
22 BGI ss105930822 Feb 05, 2009 (130)
23 1000GENOMES ss109128618 Jan 23, 2009 (130)
24 1000GENOMES ss112010206 Jan 25, 2009 (130)
25 ILLUMINA-UK ss116665920 Dec 01, 2009 (131)
26 ILLUMINA ss121762553 Dec 01, 2009 (131)
27 ENSEMBL ss143209514 Dec 01, 2009 (131)
28 ILLUMINA ss153530389 Dec 01, 2009 (131)
29 GMI ss155589430 Dec 01, 2009 (131)
30 ILLUMINA ss159288017 Dec 01, 2009 (131)
31 ILLUMINA ss160376578 Dec 01, 2009 (131)
32 COMPLETE_GENOMICS ss162359699 Jul 04, 2010 (132)
33 COMPLETE_GENOMICS ss165225289 Jul 04, 2010 (132)
34 COMPLETE_GENOMICS ss166687012 Jul 04, 2010 (132)
35 ILLUMINA ss170677096 Jul 04, 2010 (132)
36 ILLUMINA ss172594840 Jul 04, 2010 (132)
37 BUSHMAN ss200391023 Jul 04, 2010 (132)
38 BCM-HGSC-SUB ss206759546 Jul 04, 2010 (132)
39 1000GENOMES ss221742685 Jul 14, 2010 (132)
40 1000GENOMES ss232992127 Jul 14, 2010 (132)
41 1000GENOMES ss240154123 Jul 15, 2010 (132)
42 BL ss253539103 May 09, 2011 (134)
43 GMI ss278336673 May 04, 2012 (137)
44 GMI ss285197548 Apr 25, 2013 (138)
45 PJP ss293380413 May 09, 2011 (134)
46 ILLUMINA ss410908533 Sep 17, 2011 (135)
47 ILLUMINA ss480046644 May 04, 2012 (137)
48 ILLUMINA ss480055192 May 04, 2012 (137)
49 ILLUMINA ss480723678 Sep 08, 2015 (146)
50 ILLUMINA ss484821272 May 04, 2012 (137)
51 ILLUMINA ss536898929 Sep 08, 2015 (146)
52 TISHKOFF ss558466959 Apr 25, 2013 (138)
53 SSMP ss652336862 Apr 25, 2013 (138)
54 ILLUMINA ss778814538 Sep 08, 2015 (146)
55 ILLUMINA ss782857205 Sep 08, 2015 (146)
56 ILLUMINA ss783821621 Sep 08, 2015 (146)
57 ILLUMINA ss825414348 Jul 19, 2016 (147)
58 ILLUMINA ss832111163 Sep 08, 2015 (146)
59 ILLUMINA ss832800140 Jul 13, 2019 (153)
60 ILLUMINA ss834274832 Sep 08, 2015 (146)
61 EVA-GONL ss981691663 Aug 21, 2014 (142)
62 JMKIDD_LAB ss1072722917 Aug 21, 2014 (142)
63 1000GENOMES ss1315577444 Aug 21, 2014 (142)
64 DDI ss1430380533 Apr 01, 2015 (144)
65 EVA_GENOME_DK ss1581186563 Apr 01, 2015 (144)
66 EVA_DECODE ss1591211087 Apr 01, 2015 (144)
67 EVA_UK10K_ALSPAC ss1613142496 Apr 01, 2015 (144)
68 EVA_UK10K_TWINSUK ss1656136529 Apr 01, 2015 (144)
69 EVA_SVP ss1712772787 Apr 01, 2015 (144)
70 ILLUMINA ss1752583793 Sep 08, 2015 (146)
71 HAMMER_LAB ss1803677234 Sep 08, 2015 (146)
72 WEILL_CORNELL_DGM ss1924948813 Feb 12, 2016 (147)
73 ILLUMINA ss1946146650 Feb 12, 2016 (147)
74 ILLUMINA ss1958795291 Feb 12, 2016 (147)
75 GENOMED ss1970115723 Jul 19, 2016 (147)
76 JJLAB ss2023079655 Sep 14, 2016 (149)
77 ILLUMINA ss2095157615 Dec 20, 2016 (150)
78 USC_VALOUEV ss2151234886 Dec 20, 2016 (150)
79 HUMAN_LONGEVITY ss2274695601 Dec 20, 2016 (150)
80 SYSTEMSBIOZJU ss2626036245 Nov 08, 2017 (151)
81 ILLUMINA ss2634293132 Nov 08, 2017 (151)
82 GRF ss2706782596 Nov 08, 2017 (151)
83 ILLUMINA ss2711040644 Nov 08, 2017 (151)
84 GNOMAD ss2826027734 Nov 08, 2017 (151)
85 AFFY ss2985323893 Nov 08, 2017 (151)
86 AFFY ss2985954753 Nov 08, 2017 (151)
87 SWEGEN ss2997133223 Nov 08, 2017 (151)
88 ILLUMINA ss3022497705 Nov 08, 2017 (151)
89 BIOINF_KMB_FNS_UNIBA ss3025324031 Nov 08, 2017 (151)
90 CSHL ss3346442231 Nov 08, 2017 (151)
91 ILLUMINA ss3625875453 Oct 12, 2018 (152)
92 ILLUMINA ss3629259598 Oct 12, 2018 (152)
93 ILLUMINA ss3632219593 Oct 12, 2018 (152)
94 ILLUMINA ss3633377869 Oct 12, 2018 (152)
95 ILLUMINA ss3634098593 Oct 12, 2018 (152)
96 ILLUMINA ss3635006517 Oct 12, 2018 (152)
97 ILLUMINA ss3635780559 Oct 12, 2018 (152)
98 ILLUMINA ss3636718620 Oct 12, 2018 (152)
99 ILLUMINA ss3637533177 Oct 12, 2018 (152)
100 ILLUMINA ss3638559931 Oct 12, 2018 (152)
101 ILLUMINA ss3639282610 Oct 12, 2018 (152)
102 ILLUMINA ss3639664736 Oct 12, 2018 (152)
103 ILLUMINA ss3640713810 Oct 12, 2018 (152)
104 ILLUMINA ss3643505548 Oct 12, 2018 (152)
105 ILLUMINA ss3644879596 Oct 12, 2018 (152)
106 URBANLAB ss3648089847 Oct 12, 2018 (152)
107 ILLUMINA ss3652994428 Oct 12, 2018 (152)
108 ILLUMINA ss3654097595 Oct 12, 2018 (152)
109 EGCUT_WGS ss3665010528 Jul 13, 2019 (153)
110 EVA_DECODE ss3714916820 Jul 13, 2019 (153)
111 ILLUMINA ss3726241115 Jul 13, 2019 (153)
112 ACPOP ss3732459860 Jul 13, 2019 (153)
113 ILLUMINA ss3744254428 Jul 13, 2019 (153)
114 ILLUMINA ss3745306735 Jul 13, 2019 (153)
115 EVA ss3763574369 Jul 13, 2019 (153)
116 PAGE_CC ss3771208552 Jul 13, 2019 (153)
117 ILLUMINA ss3772800879 Jul 13, 2019 (153)
118 PACBIO ss3785143837 Jul 13, 2019 (153)
119 PACBIO ss3790545022 Jul 13, 2019 (153)
120 PACBIO ss3795421590 Jul 13, 2019 (153)
121 KHV_HUMAN_GENOMES ss3806741852 Jul 13, 2019 (153)
122 EVA ss3829303655 Apr 26, 2020 (154)
123 EVA ss3838125687 Apr 26, 2020 (154)
124 EVA ss3843566487 Apr 26, 2020 (154)
125 HGDP ss3847794385 Apr 26, 2020 (154)
126 SGDP_PRJ ss3862116315 Apr 26, 2020 (154)
127 KRGDB ss3908679755 Apr 26, 2020 (154)
128 KOGIC ss3956905550 Apr 26, 2020 (154)
129 EVA ss3984548672 Apr 26, 2021 (155)
130 EVA ss3985148018 Apr 26, 2021 (155)
131 EVA ss4017212565 Apr 26, 2021 (155)
132 TOPMED ss4664197768 Apr 26, 2021 (155)
133 TOMMO_GENOMICS ss5172304425 Apr 26, 2021 (155)
134 1000G_HIGH_COVERAGE ss5264400057 Oct 13, 2022 (156)
135 EVA ss5315059628 Oct 13, 2022 (156)
136 EVA ss5358346321 Oct 13, 2022 (156)
137 HUGCELL_USP ss5462531400 Oct 13, 2022 (156)
138 EVA ss5508066089 Oct 13, 2022 (156)
139 1000G_HIGH_COVERAGE ss5548273827 Oct 13, 2022 (156)
140 SANFORD_IMAGENETICS ss5638049102 Oct 13, 2022 (156)
141 TOMMO_GENOMICS ss5708861389 Oct 13, 2022 (156)
142 EVA ss5799651787 Oct 13, 2022 (156)
143 YY_MCH ss5806423832 Oct 13, 2022 (156)
144 EVA ss5835090499 Oct 13, 2022 (156)
145 EVA ss5854860822 Oct 13, 2022 (156)
146 EVA ss5894666821 Oct 13, 2022 (156)
147 EVA ss5966478406 Oct 13, 2022 (156)
148 EVA ss5979742903 Oct 13, 2022 (156)
149 1000Genomes NC_000005.9 - 73486650 Oct 12, 2018 (152)
150 1000Genomes_30x NC_000005.10 - 74190825 Oct 13, 2022 (156)
151 The Avon Longitudinal Study of Parents and Children NC_000005.9 - 73486650 Oct 12, 2018 (152)
152 Genetic variation in the Estonian population NC_000005.9 - 73486650 Oct 12, 2018 (152)
153 The Danish reference pan genome NC_000005.9 - 73486650 Apr 26, 2020 (154)
154 gnomAD - Genomes NC_000005.10 - 74190825 Apr 26, 2021 (155)
155 Genome of the Netherlands Release 5 NC_000005.9 - 73486650 Apr 26, 2020 (154)
156 HGDP-CEPH-db Supplement 1 NC_000005.8 - 73522406 Apr 26, 2020 (154)
157 HapMap NC_000005.10 - 74190825 Apr 26, 2020 (154)
158 KOREAN population from KRGDB NC_000005.9 - 73486650 Apr 26, 2020 (154)
159 Korean Genome Project NC_000005.10 - 74190825 Apr 26, 2020 (154)
160 Northern Sweden NC_000005.9 - 73486650 Jul 13, 2019 (153)
161 The PAGE Study NC_000005.10 - 74190825 Jul 13, 2019 (153)
162 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000005.9 - 73486650 Apr 26, 2021 (155)
163 CNV burdens in cranial meningiomas NC_000005.9 - 73486650 Apr 26, 2021 (155)
164 Qatari NC_000005.9 - 73486650 Apr 26, 2020 (154)
165 SGDP_PRJ NC_000005.9 - 73486650 Apr 26, 2020 (154)
166 Siberian NC_000005.9 - 73486650 Apr 26, 2020 (154)
167 8.3KJPN NC_000005.9 - 73486650 Apr 26, 2021 (155)
168 14KJPN NC_000005.10 - 74190825 Oct 13, 2022 (156)
169 TopMed NC_000005.10 - 74190825 Apr 26, 2021 (155)
170 UK 10K study - Twins NC_000005.9 - 73486650 Oct 12, 2018 (152)
171 A Vietnamese Genetic Variation Database NC_000005.9 - 73486650 Jul 13, 2019 (153)
172 ALFA NC_000005.10 - 74190825 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)
rs52813287 Sep 21, 2007 (128)
rs59463583 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
6523338634 NC_000005.10:74190824:G:A NC_000005.10:74190824:G:A (self)
15857149, ss3908679755 NC_000005.9:73486649:G:C NC_000005.10:74190824:G:C (self)
472277, ss78035046, ss93136862, ss109128618, ss112010206, ss116665920, ss162359699, ss165225289, ss166687012, ss200391023, ss206759546, ss253539103, ss278336673, ss285197548, ss293380413, ss480046644, ss825414348, ss1591211087, ss1712772787, ss3639282610, ss3639664736, ss3643505548, ss3847794385 NC_000005.8:73522405:G:T NC_000005.10:74190824:G:T (self)
27195036, 15119561, 10748776, 7351502, 6721485, 15857149, 5744725, 373945, 98040, 6990743, 14133295, 3751240, 30273732, 15119561, 3356156, ss221742685, ss232992127, ss240154123, ss480055192, ss480723678, ss484821272, ss536898929, ss558466959, ss652336862, ss778814538, ss782857205, ss783821621, ss832111163, ss832800140, ss834274832, ss981691663, ss1072722917, ss1315577444, ss1430380533, ss1581186563, ss1613142496, ss1656136529, ss1752583793, ss1803677234, ss1924948813, ss1946146650, ss1958795291, ss1970115723, ss2023079655, ss2095157615, ss2151234886, ss2626036245, ss2634293132, ss2706782596, ss2711040644, ss2826027734, ss2985323893, ss2985954753, ss2997133223, ss3022497705, ss3346442231, ss3625875453, ss3629259598, ss3632219593, ss3633377869, ss3634098593, ss3635006517, ss3635780559, ss3636718620, ss3637533177, ss3638559931, ss3640713810, ss3644879596, ss3652994428, ss3654097595, ss3665010528, ss3732459860, ss3744254428, ss3745306735, ss3763574369, ss3772800879, ss3785143837, ss3790545022, ss3795421590, ss3829303655, ss3838125687, ss3862116315, ss3908679755, ss3984548672, ss3985148018, ss4017212565, ss5172304425, ss5315059628, ss5358346321, ss5508066089, ss5638049102, ss5799651787, ss5835090499, ss5966478406, ss5979742903 NC_000005.9:73486649:G:T NC_000005.10:74190824:G:T (self)
35799762, 192248010, 2890080, 13283551, 430021, 42698493, 501575325, 6523338634, ss2274695601, ss3025324031, ss3648089847, ss3714916820, ss3726241115, ss3771208552, ss3806741852, ss3843566487, ss3956905550, ss4664197768, ss5264400057, ss5462531400, ss5548273827, ss5708861389, ss5806423832, ss5854860822, ss5894666821 NC_000005.10:74190824:G:T NC_000005.10:74190824:G:T (self)
ss11754226, ss22336671 NT_006713.13:2878781:G:T NC_000005.10:74190824:G:T (self)
ss375018, ss378225, ss570307, ss1089852, ss1091709, ss42521131, ss66830902, ss67139380, ss67480062, ss68938576, ss70445364, ss70635642, ss71186199, ss74844985, ss75879871, ss83371241, ss98734521, ss105930822, ss121762553, ss143209514, ss153530389, ss155589430, ss159288017, ss160376578, ss170677096, ss172594840, ss410908533 NT_006713.15:24081008:G:T NC_000005.10:74190824: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 rs158805

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