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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.

rs808225

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr14:57931198 (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=0.489550 (129579/264690, TOPMED)
G=0.443765 (105538/237824, ALFA)
G=0.498221 (69715/139928, GnomAD) (+ 23 more)
A=0.42809 (33688/78694, PAGE_STUDY)
A=0.26966 (7620/28258, 14KJPN)
A=0.26814 (4494/16760, 8.3KJPN)
A=0.4386 (2809/6404, 1000G_30x)
A=0.4379 (2193/5008, 1000G)
G=0.4018 (1800/4480, Estonian)
G=0.4292 (1654/3854, ALSPAC)
G=0.4177 (1549/3708, TWINSUK)
A=0.2580 (756/2930, KOREAN)
A=0.4519 (940/2080, HGDP_Stanford)
A=0.3940 (743/1886, HapMap)
A=0.2418 (443/1832, Korea1K)
G=0.4074 (462/1134, Daghestan)
G=0.432 (431/998, GoNL)
A=0.247 (191/774, PRJEB37584)
G=0.364 (228/626, Chileans)
G=0.402 (241/600, NorthernSweden)
A=0.292 (118/404, SGDP_PRJ)
G=0.495 (107/216, Qatari)
A=0.176 (38/216, Vietnamese)
A=0.48 (32/66, Ancient Sardinia)
G=0.33 (13/40, GENOME_DK)
A=0.31 (11/36, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
SLC35F4 : Intron Variant
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 238040 A=0.556201 G=0.443799
European Sub 200936 A=0.576452 G=0.423548
African Sub 9250 A=0.3430 G=0.6570
African Others Sub 320 A=0.325 G=0.675
African American Sub 8930 A=0.3437 G=0.6563
Asian Sub 6400 A=0.2578 G=0.7422
East Asian Sub 4540 A=0.2311 G=0.7689
Other Asian Sub 1860 A=0.3231 G=0.6769
Latin American 1 Sub 696 A=0.527 G=0.473
Latin American 2 Sub 3732 A=0.5962 G=0.4038
South Asian Sub 5152 A=0.6231 G=0.3769
Other Sub 11874 A=0.50051 G=0.49949


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=0.489550 G=0.510450
Allele Frequency Aggregator Total Global 237824 A=0.556235 G=0.443765
Allele Frequency Aggregator European Sub 200756 A=0.576491 G=0.423509
Allele Frequency Aggregator Other Sub 11852 A=0.50067 G=0.49933
Allele Frequency Aggregator African Sub 9236 A=0.3428 G=0.6572
Allele Frequency Aggregator Asian Sub 6400 A=0.2578 G=0.7422
Allele Frequency Aggregator South Asian Sub 5152 A=0.6231 G=0.3769
Allele Frequency Aggregator Latin American 2 Sub 3732 A=0.5962 G=0.4038
Allele Frequency Aggregator Latin American 1 Sub 696 A=0.527 G=0.473
gnomAD - Genomes Global Study-wide 139928 A=0.501779 G=0.498221
gnomAD - Genomes European Sub 75794 A=0.58927 G=0.41073
gnomAD - Genomes African Sub 41902 A=0.34304 G=0.65696
gnomAD - Genomes American Sub 13636 A=0.58859 G=0.41141
gnomAD - Genomes Ashkenazi Jewish Sub 3320 A=0.4157 G=0.5843
gnomAD - Genomes East Asian Sub 3124 A=0.2382 G=0.7618
gnomAD - Genomes Other Sub 2152 A=0.4768 G=0.5232
The PAGE Study Global Study-wide 78694 A=0.42809 G=0.57191
The PAGE Study AfricanAmerican Sub 32514 A=0.34385 G=0.65615
The PAGE Study Mexican Sub 10810 A=0.58677 G=0.41323
The PAGE Study Asian Sub 8314 A=0.2658 G=0.7342
The PAGE Study PuertoRican Sub 7916 A=0.5202 G=0.4798
The PAGE Study NativeHawaiian Sub 4534 A=0.4581 G=0.5419
The PAGE Study Cuban Sub 4230 A=0.5395 G=0.4605
The PAGE Study Dominican Sub 3828 A=0.4577 G=0.5423
The PAGE Study CentralAmerican Sub 2450 A=0.5604 G=0.4396
The PAGE Study SouthAmerican Sub 1982 A=0.5853 G=0.4147
The PAGE Study NativeAmerican Sub 1260 A=0.5556 G=0.4444
The PAGE Study SouthAsian Sub 856 A=0.576 G=0.424
14KJPN JAPANESE Study-wide 28258 A=0.26966 G=0.73034
8.3KJPN JAPANESE Study-wide 16760 A=0.26814 G=0.73186
1000Genomes_30x Global Study-wide 6404 A=0.4386 G=0.5614
1000Genomes_30x African Sub 1786 A=0.2912 G=0.7088
1000Genomes_30x Europe Sub 1266 A=0.5956 G=0.4044
1000Genomes_30x South Asian Sub 1202 A=0.5749 G=0.4251
1000Genomes_30x East Asian Sub 1170 A=0.2470 G=0.7530
1000Genomes_30x American Sub 980 A=0.566 G=0.434
1000Genomes Global Study-wide 5008 A=0.4379 G=0.5621
1000Genomes African Sub 1322 A=0.2920 G=0.7080
1000Genomes East Asian Sub 1008 A=0.2450 G=0.7550
1000Genomes Europe Sub 1006 A=0.5974 G=0.4026
1000Genomes South Asian Sub 978 A=0.571 G=0.429
1000Genomes American Sub 694 A=0.578 G=0.422
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.5982 G=0.4018
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.5708 G=0.4292
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.5823 G=0.4177
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.2580 G=0.7420
HGDP-CEPH-db Supplement 1 Global Study-wide 2080 A=0.4519 G=0.5481
HGDP-CEPH-db Supplement 1 Est_Asia Sub 468 A=0.248 G=0.752
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.543 G=0.457
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.503 G=0.497
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.559 G=0.441
HGDP-CEPH-db Supplement 1 Africa Sub 242 A=0.269 G=0.731
HGDP-CEPH-db Supplement 1 America Sub 214 A=0.631 G=0.369
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.61 G=0.39
HapMap Global Study-wide 1886 A=0.3940 G=0.6060
HapMap American Sub 768 A=0.473 G=0.527
HapMap African Sub 688 A=0.299 G=0.701
HapMap Asian Sub 254 A=0.276 G=0.724
HapMap Europe Sub 176 A=0.591 G=0.409
Korean Genome Project KOREAN Study-wide 1832 A=0.2418 G=0.7582
Genome-wide autozygosity in Daghestan Global Study-wide 1134 A=0.5926 G=0.4074
Genome-wide autozygosity in Daghestan Daghestan Sub 626 A=0.636 G=0.364
Genome-wide autozygosity in Daghestan Near_East Sub 144 A=0.549 G=0.451
Genome-wide autozygosity in Daghestan Central Asia Sub 122 A=0.508 G=0.492
Genome-wide autozygosity in Daghestan Europe Sub 108 A=0.583 G=0.417
Genome-wide autozygosity in Daghestan South Asian Sub 98 A=0.54 G=0.46
Genome-wide autozygosity in Daghestan Caucasus Sub 36 A=0.47 G=0.53
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.568 G=0.432
CNV burdens in cranial meningiomas Global Study-wide 774 A=0.247 G=0.753
CNV burdens in cranial meningiomas CRM Sub 774 A=0.247 G=0.753
Chileans Chilean Study-wide 626 A=0.636 G=0.364
Northern Sweden ACPOP Study-wide 600 A=0.598 G=0.402
SGDP_PRJ Global Study-wide 404 A=0.292 G=0.708
Qatari Global Study-wide 216 A=0.505 G=0.495
A Vietnamese Genetic Variation Database Global Study-wide 216 A=0.176 G=0.824
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 66 A=0.48 G=0.52
The Danish reference pan genome Danish Study-wide 40 A=0.68 G=0.33
Siberian Global Study-wide 36 A=0.31 G=0.69
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 14 NC_000014.9:g.57931198A>G
GRCh37.p13 chr 14 NC_000014.8:g.58397916A>G
Gene: SLC35F4, solute carrier family 35 member F4 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
SLC35F4 transcript variant 2 NM_001206920.2:c. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant 1 NM_001306087.2:c. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant 3 NM_001352011.2:c. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant 4 NM_001352012.2:c. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant 5 NM_001352013.2:c. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant 6 NM_001352014.2:c. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant 7 NM_001352015.3:c. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant 8 NM_001352016.2:c. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant 9 NR_159373.2:n. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant 10 NR_159374.2:n. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant 11 NR_159375.2:n. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant 12 NR_159376.2:n. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant X3 XM_011536723.4:c.64+50715…

XM_011536723.4:c.64+50715T>C

 		N/A Intron Variant
SLC35F4 transcript variant X1 XM_011536720.4:c. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant X2 XM_011536721.4:c. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant X4 XM_011536724.4:c. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant X9 XM_024449561.2:c. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant X8 XM_047431343.1:c. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant X7 XR_002957548.2:n. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant X5 XR_007064010.1:n. N/A Genic Upstream Transcript Variant
SLC35F4 transcript variant X6 XR_943418.4:n. N/A Genic Upstream 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 A= G
GRCh38.p14 chr 14 NC_000014.9:g.57931198= NC_000014.9:g.57931198A>G
GRCh37.p13 chr 14 NC_000014.8:g.58397916= NC_000014.8:g.58397916A>G
SLC35F4 transcript variant X3 XM_011536723.4:c.64+50715= XM_011536723.4:c.64+50715T>C
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#.

133 SubSNP, 26 Frequency submissions
No Submitter Submission ID Date (Build)
1 KWOK ss1044637 Oct 05, 2000 (86)
2 SC_JCM ss3877966 Sep 28, 2001 (100)
3 WI_SSAHASNP ss14382418 Dec 05, 2003 (119)
4 CSHL-HAPMAP ss19988498 Feb 27, 2004 (120)
5 ABI ss40512001 Mar 14, 2006 (126)
6 AFFY ss65995100 Nov 30, 2006 (127)
7 AFFY ss66529265 Nov 30, 2006 (127)
8 ILLUMINA ss66596604 Nov 30, 2006 (127)
9 ILLUMINA ss67869530 Nov 30, 2006 (127)
10 ILLUMINA ss68015142 Nov 30, 2006 (127)
11 ILLUMINA ss70969384 May 27, 2008 (130)
12 ILLUMINA ss71579762 May 17, 2007 (127)
13 ILLUMINA ss74945469 Dec 06, 2007 (129)
14 AFFY ss76351795 Dec 06, 2007 (129)
15 ILLUMINA ss79280806 Dec 16, 2007 (130)
16 HGSV ss82167633 Dec 16, 2007 (130)
17 KRIBB_YJKIM ss83569066 Dec 16, 2007 (130)
18 HGSV ss84941164 Dec 16, 2007 (130)
19 BCMHGSC_JDW ss89961831 Mar 24, 2008 (129)
20 HUMANGENOME_JCVI ss96920813 Feb 06, 2009 (130)
21 BGI ss106390960 Feb 06, 2009 (130)
22 ILLUMINA-UK ss118502558 Feb 14, 2009 (130)
23 ILLUMINA ss122898806 Dec 01, 2009 (131)
24 ENSEMBL ss132329522 Dec 01, 2009 (131)
25 ENSEMBL ss133996317 Dec 01, 2009 (131)
26 ILLUMINA ss154467984 Dec 01, 2009 (131)
27 GMI ss155853696 Dec 01, 2009 (131)
28 ILLUMINA ss159642506 Dec 01, 2009 (131)
29 ILLUMINA ss172395617 Jul 04, 2010 (132)
30 AFFY ss173354956 Jul 04, 2010 (132)
31 ILLUMINA ss174710881 Jul 04, 2010 (132)
32 BUSHMAN ss200128919 Jul 04, 2010 (132)
33 BCM-HGSC-SUB ss206863497 Jul 04, 2010 (132)
34 1000GENOMES ss210859355 Jul 14, 2010 (132)
35 1000GENOMES ss211525028 Jul 14, 2010 (132)
36 1000GENOMES ss226593546 Jul 14, 2010 (132)
37 1000GENOMES ss236558932 Jul 15, 2010 (132)
38 1000GENOMES ss242989775 Jul 15, 2010 (132)
39 BL ss255021221 May 09, 2011 (134)
40 GMI ss282021307 May 04, 2012 (137)
41 GMI ss286849821 Apr 25, 2013 (138)
42 PJP ss291609659 May 09, 2011 (134)
43 EXOME_CHIP ss491485369 May 04, 2012 (137)
44 ILLUMINA ss537553520 Sep 08, 2015 (146)
45 TISHKOFF ss564119657 Apr 25, 2013 (138)
46 SSMP ss659800567 Apr 25, 2013 (138)
47 ILLUMINA ss780687026 Sep 08, 2015 (146)
48 ILLUMINA ss783360569 Sep 08, 2015 (146)
49 ILLUMINA ss825611324 Jul 19, 2016 (147)
50 ILLUMINA ss833153352 Jul 13, 2019 (153)
51 EVA-GONL ss991192574 Aug 21, 2014 (142)
52 JMKIDD_LAB ss1079689891 Aug 21, 2014 (142)
53 1000GENOMES ss1351180537 Aug 21, 2014 (142)
54 HAMMER_LAB ss1397681819 Sep 08, 2015 (146)
55 DDI ss1427438550 Apr 01, 2015 (144)
56 EVA_GENOME_DK ss1577282991 Apr 01, 2015 (144)
57 EVA_UK10K_ALSPAC ss1631826536 Apr 01, 2015 (144)
58 EVA_UK10K_TWINSUK ss1674820569 Apr 01, 2015 (144)
59 EVA_DECODE ss1695193133 Apr 01, 2015 (144)
60 EVA_SVP ss1713447802 Apr 01, 2015 (144)
61 ILLUMINA ss1752136270 Sep 08, 2015 (146)
62 HAMMER_LAB ss1807943365 Sep 08, 2015 (146)
63 ILLUMINA ss1917888940 Feb 12, 2016 (147)
64 WEILL_CORNELL_DGM ss1934569119 Feb 12, 2016 (147)
65 ILLUMINA ss1946377815 Feb 12, 2016 (147)
66 ILLUMINA ss1959557732 Feb 12, 2016 (147)
67 GENOMED ss1967973455 Jul 19, 2016 (147)
68 JJLAB ss2028062202 Sep 14, 2016 (149)
69 USC_VALOUEV ss2156437339 Dec 20, 2016 (150)
70 HUMAN_LONGEVITY ss2202340963 Dec 20, 2016 (150)
71 SYSTEMSBIOZJU ss2628521302 Nov 08, 2017 (151)
72 ILLUMINA ss2633156038 Nov 08, 2017 (151)
73 ILLUMINA ss2633156039 Nov 08, 2017 (151)
74 GRF ss2700863223 Nov 08, 2017 (151)
75 GNOMAD ss2928193812 Nov 08, 2017 (151)
76 AFFY ss2985022649 Nov 08, 2017 (151)
77 AFFY ss2985655983 Nov 08, 2017 (151)
78 SWEGEN ss3012273260 Nov 08, 2017 (151)
79 ILLUMINA ss3021572879 Nov 08, 2017 (151)
80 BIOINF_KMB_FNS_UNIBA ss3027856770 Nov 08, 2017 (151)
81 CSHL ss3350827510 Nov 08, 2017 (151)
82 ILLUMINA ss3627228287 Oct 12, 2018 (152)
83 ILLUMINA ss3627228288 Oct 12, 2018 (152)
84 ILLUMINA ss3634578667 Oct 12, 2018 (152)
85 ILLUMINA ss3638052882 Oct 12, 2018 (152)
86 ILLUMINA ss3639039981 Oct 12, 2018 (152)
87 ILLUMINA ss3639524691 Oct 12, 2018 (152)
88 ILLUMINA ss3640285994 Oct 12, 2018 (152)
89 ILLUMINA ss3643039343 Oct 12, 2018 (152)
90 ILLUMINA ss3644630930 Oct 12, 2018 (152)
91 URBANLAB ss3650216840 Oct 12, 2018 (152)
92 ILLUMINA ss3651965942 Oct 12, 2018 (152)
93 ILLUMINA ss3653793617 Oct 12, 2018 (152)
94 EGCUT_WGS ss3679522941 Jul 13, 2019 (153)
95 EVA_DECODE ss3696765788 Jul 13, 2019 (153)
96 ILLUMINA ss3725451366 Jul 13, 2019 (153)
97 ACPOP ss3740420984 Jul 13, 2019 (153)
98 ILLUMINA ss3744412072 Jul 13, 2019 (153)
99 ILLUMINA ss3744879268 Jul 13, 2019 (153)
100 EVA ss3752375945 Jul 13, 2019 (153)
101 PAGE_CC ss3771791602 Jul 13, 2019 (153)
102 ILLUMINA ss3772378115 Jul 13, 2019 (153)
103 PACBIO ss3787676876 Jul 13, 2019 (153)
104 PACBIO ss3792713792 Jul 13, 2019 (153)
105 PACBIO ss3797598009 Jul 13, 2019 (153)
106 KHV_HUMAN_GENOMES ss3817709350 Jul 13, 2019 (153)
107 EVA ss3833943042 Apr 27, 2020 (154)
108 EVA ss3840565069 Apr 27, 2020 (154)
109 EVA ss3846054190 Apr 27, 2020 (154)
110 HGDP ss3847504804 Apr 27, 2020 (154)
111 SGDP_PRJ ss3881600399 Apr 27, 2020 (154)
112 KRGDB ss3930621627 Apr 27, 2020 (154)
113 KOGIC ss3975013751 Apr 27, 2020 (154)
114 EVA ss3984692174 Apr 26, 2021 (155)
115 EVA ss3985682306 Apr 26, 2021 (155)
116 EVA ss4017672383 Apr 26, 2021 (155)
117 TOPMED ss4972161807 Apr 26, 2021 (155)
118 TOMMO_GENOMICS ss5213430130 Apr 26, 2021 (155)
119 1000G_HIGH_COVERAGE ss5296378709 Oct 16, 2022 (156)
120 EVA ss5315739999 Oct 16, 2022 (156)
121 EVA ss5415544947 Oct 16, 2022 (156)
122 HUGCELL_USP ss5490405725 Oct 16, 2022 (156)
123 1000G_HIGH_COVERAGE ss5596740255 Oct 16, 2022 (156)
124 SANFORD_IMAGENETICS ss5624344871 Oct 16, 2022 (156)
125 SANFORD_IMAGENETICS ss5656310983 Oct 16, 2022 (156)
126 TOMMO_GENOMICS ss5766289161 Oct 16, 2022 (156)
127 YY_MCH ss5814791123 Oct 16, 2022 (156)
128 EVA ss5841168132 Oct 16, 2022 (156)
129 EVA ss5847437992 Oct 16, 2022 (156)
130 EVA ss5851051637 Oct 16, 2022 (156)
131 EVA ss5901516996 Oct 16, 2022 (156)
132 EVA ss5947743883 Oct 16, 2022 (156)
133 EVA ss5979442029 Oct 16, 2022 (156)
134 1000Genomes NC_000014.8 - 58397916 Oct 12, 2018 (152)
135 1000Genomes_30x NC_000014.9 - 57931198 Oct 16, 2022 (156)
136 The Avon Longitudinal Study of Parents and Children NC_000014.8 - 58397916 Oct 12, 2018 (152)
137 Chileans NC_000014.8 - 58397916 Apr 27, 2020 (154)
138 Genome-wide autozygosity in Daghestan NC_000014.7 - 57467669 Apr 27, 2020 (154)
139 Genetic variation in the Estonian population NC_000014.8 - 58397916 Oct 12, 2018 (152)
140 The Danish reference pan genome NC_000014.8 - 58397916 Apr 27, 2020 (154)
141 gnomAD - Genomes NC_000014.9 - 57931198 Apr 26, 2021 (155)
142 Genome of the Netherlands Release 5 NC_000014.8 - 58397916 Apr 27, 2020 (154)
143 HGDP-CEPH-db Supplement 1 NC_000014.7 - 57467669 Apr 27, 2020 (154)
144 HapMap NC_000014.9 - 57931198 Apr 27, 2020 (154)
145 KOREAN population from KRGDB NC_000014.8 - 58397916 Apr 27, 2020 (154)
146 Korean Genome Project NC_000014.9 - 57931198 Apr 27, 2020 (154)
147 Northern Sweden NC_000014.8 - 58397916 Jul 13, 2019 (153)
148 The PAGE Study NC_000014.9 - 57931198 Jul 13, 2019 (153)
149 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000014.8 - 58397916 Apr 26, 2021 (155)
150 CNV burdens in cranial meningiomas NC_000014.8 - 58397916 Apr 26, 2021 (155)
151 Qatari NC_000014.8 - 58397916 Apr 27, 2020 (154)
152 SGDP_PRJ NC_000014.8 - 58397916 Apr 27, 2020 (154)
153 Siberian NC_000014.8 - 58397916 Apr 27, 2020 (154)
154 8.3KJPN NC_000014.8 - 58397916 Apr 26, 2021 (155)
155 14KJPN NC_000014.9 - 57931198 Oct 16, 2022 (156)
156 TopMed NC_000014.9 - 57931198 Apr 26, 2021 (155)
157 UK 10K study - Twins NC_000014.8 - 58397916 Oct 12, 2018 (152)
158 A Vietnamese Genetic Variation Database NC_000014.8 - 58397916 Jul 13, 2019 (153)
159 ALFA NC_000014.9 - 57931198 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)
rs61695403 May 27, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
152163, 182696, ss66529265, ss76351795, ss82167633, ss84941164, ss89961831, ss118502558, ss173354956, ss200128919, ss206863497, ss210859355, ss211525028, ss255021221, ss282021307, ss286849821, ss291609659, ss825611324, ss1397681819, ss1695193133, ss1713447802, ss3639039981, ss3639524691, ss3643039343, ss3847504804 NC_000014.7:57467668:A:G NC_000014.9:57931197:A:G (self)
64167878, 35644394, 139158, 25261189, 3621884, 15922413, 37799021, 13705849, 908233, 241690, 16611049, 33617379, 8953693, 71399437, 35644394, 7930956, ss226593546, ss236558932, ss242989775, ss491485369, ss537553520, ss564119657, ss659800567, ss780687026, ss783360569, ss833153352, ss991192574, ss1079689891, ss1351180537, ss1427438550, ss1577282991, ss1631826536, ss1674820569, ss1752136270, ss1807943365, ss1917888940, ss1934569119, ss1946377815, ss1959557732, ss1967973455, ss2028062202, ss2156437339, ss2628521302, ss2633156038, ss2633156039, ss2700863223, ss2928193812, ss2985022649, ss2985655983, ss3012273260, ss3021572879, ss3350827510, ss3627228287, ss3627228288, ss3634578667, ss3638052882, ss3640285994, ss3644630930, ss3651965942, ss3653793617, ss3679522941, ss3740420984, ss3744412072, ss3744879268, ss3752375945, ss3772378115, ss3787676876, ss3792713792, ss3797598009, ss3833943042, ss3840565069, ss3881600399, ss3930621627, ss3984692174, ss3985682306, ss4017672383, ss5213430130, ss5315739999, ss5415544947, ss5624344871, ss5656310983, ss5841168132, ss5847437992, ss5947743883, ss5979442029 NC_000014.8:58397915:A:G NC_000014.9:57931197:A:G (self)
84266190, 452444732, 1154058, 31391752, 1013071, 100126265, 187707466, 2702735958, ss2202340963, ss3027856770, ss3650216840, ss3696765788, ss3725451366, ss3771791602, ss3817709350, ss3846054190, ss3975013751, ss4972161807, ss5296378709, ss5490405725, ss5596740255, ss5766289161, ss5814791123, ss5851051637, ss5901516996 NC_000014.9:57931197:A:G NC_000014.9:57931197:A:G (self)
ss14382418, ss19988498 NT_026437.10:38317956:A:G NC_000014.9:57931197:A:G (self)
ss1044637, ss3877966, ss40512001, ss65995100, ss66596604, ss67869530, ss68015142, ss70969384, ss71579762, ss74945469, ss79280806, ss83569066, ss96920813, ss106390960, ss122898806, ss132329522, ss133996317, ss154467984, ss155853696, ss159642506, ss172395617, ss174710881 NT_026437.12:39397915:A:G NC_000014.9:57931197: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 rs808225
PMID Title Author Year Journal
17903307 Framingham Heart Study genome-wide association: results for pulmonary function measures. Wilk JB et al. 2007 BMC medical genetics
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