Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

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.

rs7219690

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr17:76555886 (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>A / C>G / C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.028701 (8487/295706, ALFA)
C=0.159069 (42104/264690, TOPMED)
C=0.149755 (20986/140136, GnomAD) (+ 21 more)
C=0.22750 (17899/78676, PAGE_STUDY)
C=0.00000 (0/28258, 14KJPN)
C=0.00000 (0/16760, 8.3KJPN)
C=0.1576 (1009/6404, 1000G_30x)
C=0.1502 (752/5008, 1000G)
C=0.0038 (17/4480, Estonian)
C=0.0135 (52/3854, ALSPAC)
C=0.0119 (44/3708, TWINSUK)
C=0.0003 (1/2930, KOREAN)
C=0.0921 (192/2084, HGDP_Stanford)
C=0.0000 (0/1832, Korea1K)
C=0.2770 (379/1368, HapMap)
C=0.009 (9/998, GoNL)
C=0.000 (0/792, PRJEB37584)
C=0.007 (4/600, NorthernSweden)
C=0.037 (19/520, SGDP_PRJ)
C=0.144 (31/216, Qatari)
C=0.000 (0/214, Vietnamese)
C=0.00 (0/90, Ancient Sardinia)
C=0.00 (0/56, Siberian)
C=0.00 (0/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
SNHG16 : 2KB Upstream 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 295706 C=0.028701 T=0.971299
European Sub 259844 C=0.014351 T=0.985649
African Sub 8496 C=0.4450 T=0.5550
African Others Sub 322 C=0.509 T=0.491
African American Sub 8174 C=0.4425 T=0.5575
Asian Sub 3972 C=0.0000 T=1.0000
East Asian Sub 3194 C=0.0000 T=1.0000
Other Asian Sub 778 C=0.000 T=1.000
Latin American 1 Sub 1216 C=0.1554 T=0.8446
Latin American 2 Sub 8384 C=0.0340 T=0.9660
South Asian Sub 5234 C=0.0031 T=0.9969
Other Sub 8560 C=0.0569 T=0.9431


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 295706 C=0.028701 T=0.971299
Allele Frequency Aggregator European Sub 259844 C=0.014351 T=0.985649
Allele Frequency Aggregator Other Sub 8560 C=0.0569 T=0.9431
Allele Frequency Aggregator African Sub 8496 C=0.4450 T=0.5550
Allele Frequency Aggregator Latin American 2 Sub 8384 C=0.0340 T=0.9660
Allele Frequency Aggregator South Asian Sub 5234 C=0.0031 T=0.9969
Allele Frequency Aggregator Asian Sub 3972 C=0.0000 T=1.0000
Allele Frequency Aggregator Latin American 1 Sub 1216 C=0.1554 T=0.8446
TopMed Global Study-wide 264690 C=0.159069 T=0.840931
gnomAD - Genomes Global Study-wide 140136 C=0.149755 T=0.850245
gnomAD - Genomes European Sub 75964 C=0.01085 T=0.98915
gnomAD - Genomes African Sub 41900 C=0.44897 T=0.55103
gnomAD - Genomes American Sub 13666 C=0.06527 T=0.93473
gnomAD - Genomes Ashkenazi Jewish Sub 3324 C=0.0560 T=0.9440
gnomAD - Genomes East Asian Sub 3134 C=0.0000 T=1.0000
gnomAD - Genomes Other Sub 2148 C=0.1266 T=0.8734
The PAGE Study Global Study-wide 78676 C=0.22750 T=0.77250
The PAGE Study AfricanAmerican Sub 32508 C=0.43497 T=0.56503
The PAGE Study Mexican Sub 10804 C=0.03850 T=0.96150
The PAGE Study Asian Sub 8316 C=0.0005 T=0.9995
The PAGE Study PuertoRican Sub 7916 C=0.1709 T=0.8291
The PAGE Study NativeHawaiian Sub 4534 C=0.0146 T=0.9854
The PAGE Study Cuban Sub 4224 C=0.1094 T=0.8906
The PAGE Study Dominican Sub 3828 C=0.2652 T=0.7348
The PAGE Study CentralAmerican Sub 2450 C=0.0898 T=0.9102
The PAGE Study SouthAmerican Sub 1980 C=0.0576 T=0.9424
The PAGE Study NativeAmerican Sub 1260 C=0.0841 T=0.9159
The PAGE Study SouthAsian Sub 856 C=0.004 T=0.996
14KJPN JAPANESE Study-wide 28258 C=0.00000 T=1.00000
8.3KJPN JAPANESE Study-wide 16760 C=0.00000 T=1.00000
1000Genomes_30x Global Study-wide 6404 C=0.1576 T=0.8424
1000Genomes_30x African Sub 1786 C=0.5325 T=0.4675
1000Genomes_30x Europe Sub 1266 C=0.0071 T=0.9929
1000Genomes_30x South Asian Sub 1202 C=0.0000 T=1.0000
1000Genomes_30x East Asian Sub 1170 C=0.0000 T=1.0000
1000Genomes_30x American Sub 980 C=0.050 T=0.950
1000Genomes Global Study-wide 5008 C=0.1502 T=0.8498
1000Genomes African Sub 1322 C=0.5325 T=0.4675
1000Genomes East Asian Sub 1008 C=0.0000 T=1.0000
1000Genomes Europe Sub 1006 C=0.0080 T=0.9920
1000Genomes South Asian Sub 978 C=0.001 T=0.999
1000Genomes American Sub 694 C=0.056 T=0.944
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.0038 T=0.9962
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.0135 T=0.9865
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.0119 T=0.9881
KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.0003 A=0.0000, G=0.0000, T=0.9997
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 C=0.0921 T=0.9079
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 C=0.002 T=0.998
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 C=0.019 T=0.981
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 C=0.109 T=0.891
HGDP-CEPH-db Supplement 1 Europe Sub 320 C=0.016 T=0.984
HGDP-CEPH-db Supplement 1 Africa Sub 242 C=0.570 T=0.430
HGDP-CEPH-db Supplement 1 America Sub 216 C=0.009 T=0.991
HGDP-CEPH-db Supplement 1 Oceania Sub 72 C=0.00 T=1.00
Korean Genome Project KOREAN Study-wide 1832 C=0.0000 T=1.0000
HapMap Global Study-wide 1368 C=0.2770 T=0.7230
HapMap African Sub 682 C=0.487 T=0.513
HapMap American Sub 424 C=0.108 T=0.892
HapMap Europe Sub 176 C=0.006 T=0.994
HapMap Asian Sub 86 C=0.00 T=1.00
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.009 T=0.991
CNV burdens in cranial meningiomas Global Study-wide 792 C=0.000 T=1.000
CNV burdens in cranial meningiomas CRM Sub 792 C=0.000 T=1.000
Northern Sweden ACPOP Study-wide 600 C=0.007 T=0.993
SGDP_PRJ Global Study-wide 520 C=0.037 T=0.963
Qatari Global Study-wide 216 C=0.144 T=0.856
A Vietnamese Genetic Variation Database Global Study-wide 214 C=0.000 T=1.000
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 90 C=0.00 T=1.00
Siberian Global Study-wide 56 C=0.00 T=1.00
The Danish reference pan genome Danish Study-wide 40 C=0.00 T=1.00
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 17 NC_000017.11:g.76555886C>A
GRCh38.p14 chr 17 NC_000017.11:g.76555886C>G
GRCh38.p14 chr 17 NC_000017.11:g.76555886C>T
GRCh37.p13 chr 17 NC_000017.10:g.74551968C>A
GRCh37.p13 chr 17 NC_000017.10:g.74551968C>G
GRCh37.p13 chr 17 NC_000017.10:g.74551968C>T
Gene: SNHG16, small nucleolar RNA host gene 16 (plus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
SNHG16 transcript variant 1 NR_038108.1:n. N/A Upstream Transcript Variant
SNHG16 transcript variant 2 NR_038109.1:n. N/A Upstream Transcript Variant
SNHG16 transcript variant 3 NR_038110.1:n. N/A Upstream Transcript Variant
SNHG16 transcript variant 4 NR_038111.1:n. N/A 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 C= A G T
GRCh38.p14 chr 17 NC_000017.11:g.76555886= NC_000017.11:g.76555886C>A NC_000017.11:g.76555886C>G NC_000017.11:g.76555886C>T
GRCh37.p13 chr 17 NC_000017.10:g.74551968= NC_000017.10:g.74551968C>A NC_000017.10:g.74551968C>G NC_000017.10:g.74551968C>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#.

137 SubSNP, 24 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCM_SSAHASNP ss10869078 Jul 11, 2003 (116)
2 BCM_SSAHASNP ss14277620 Dec 05, 2003 (119)
3 CSHL-HAPMAP ss16745774 Feb 27, 2004 (120)
4 CSHL-HAPMAP ss20037853 Feb 27, 2004 (120)
5 SSAHASNP ss21372551 Apr 05, 2004 (121)
6 ABI ss40761401 Mar 15, 2006 (126)
7 ILLUMINA ss67557655 Dec 02, 2006 (127)
8 ILLUMINA ss67934236 Dec 02, 2006 (127)
9 ILLUMINA ss68273225 Dec 12, 2006 (127)
10 ILLUMINA ss70917082 May 24, 2008 (130)
11 ILLUMINA ss71516028 May 18, 2007 (127)
12 ILLUMINA ss75749370 Dec 05, 2007 (129)
13 AFFY ss76738131 Dec 08, 2007 (130)
14 HGSV ss77543308 Dec 05, 2007 (129)
15 HGSV ss83488624 Dec 14, 2007 (130)
16 KRIBB_YJKIM ss84640197 Dec 14, 2007 (130)
17 BCMHGSC_JDW ss90663695 Mar 24, 2008 (129)
18 BGI ss106520883 Feb 04, 2009 (130)
19 1000GENOMES ss109928038 Jan 24, 2009 (130)
20 1000GENOMES ss113851436 Jan 25, 2009 (130)
21 ENSEMBL ss136505664 Dec 01, 2009 (131)
22 ENSEMBL ss137189502 Dec 01, 2009 (131)
23 ILLUMINA ss154413550 Dec 01, 2009 (131)
24 GMI ss154651171 Dec 01, 2009 (131)
25 ILLUMINA ss159588636 Dec 01, 2009 (131)
26 ILLUMINA ss160861800 Dec 01, 2009 (131)
27 COMPLETE_GENOMICS ss168513417 Jul 04, 2010 (132)
28 COMPLETE_GENOMICS ss170252008 Jul 04, 2010 (132)
29 COMPLETE_GENOMICS ss171742660 Jul 04, 2010 (132)
30 ILLUMINA ss174296069 Jul 04, 2010 (132)
31 BCM-HGSC-SUB ss207910679 Jul 04, 2010 (132)
32 1000GENOMES ss227662602 Jul 14, 2010 (132)
33 1000GENOMES ss237325700 Jul 15, 2010 (132)
34 1000GENOMES ss243603792 Jul 15, 2010 (132)
35 BL ss255799201 May 09, 2011 (134)
36 GMI ss282845878 May 04, 2012 (137)
37 GMI ss287217395 Apr 25, 2013 (138)
38 PJP ss291996101 May 09, 2011 (134)
39 ILLUMINA ss481510913 May 04, 2012 (137)
40 ILLUMINA ss481539431 May 04, 2012 (137)
41 ILLUMINA ss482514767 Sep 08, 2015 (146)
42 ILLUMINA ss485550474 May 04, 2012 (137)
43 ILLUMINA ss537452178 Sep 08, 2015 (146)
44 TISHKOFF ss565413450 Apr 25, 2013 (138)
45 SSMP ss661227032 Apr 25, 2013 (138)
46 ILLUMINA ss783220796 Sep 08, 2015 (146)
47 ILLUMINA ss784175243 Sep 08, 2015 (146)
48 ILLUMINA ss832481025 Sep 08, 2015 (146)
49 ILLUMINA ss833099671 Jul 13, 2019 (153)
50 ILLUMINA ss834054466 Sep 08, 2015 (146)
51 EVA-GONL ss993345206 Aug 21, 2014 (142)
52 JMKIDD_LAB ss1081223287 Aug 21, 2014 (142)
53 1000GENOMES ss1359587050 Aug 21, 2014 (142)
54 DDI ss1428100192 Apr 01, 2015 (144)
55 EVA_GENOME_DK ss1578248545 Apr 01, 2015 (144)
56 EVA_UK10K_ALSPAC ss1636128727 Apr 01, 2015 (144)
57 EVA_UK10K_TWINSUK ss1679122760 Apr 01, 2015 (144)
58 EVA_DECODE ss1697396261 Apr 01, 2015 (144)
59 EVA_SVP ss1713599149 Apr 01, 2015 (144)
60 ILLUMINA ss1752240995 Sep 08, 2015 (146)
61 HAMMER_LAB ss1808885932 Sep 08, 2015 (146)
62 WEILL_CORNELL_DGM ss1936808593 Feb 12, 2016 (147)
63 ILLUMINA ss1946473862 Feb 12, 2016 (147)
64 ILLUMINA ss1959771495 Feb 12, 2016 (147)
65 GENOMED ss1968437469 Jul 19, 2016 (147)
66 JJLAB ss2029176291 Sep 14, 2016 (149)
67 USC_VALOUEV ss2157662463 Dec 20, 2016 (150)
68 HUMAN_LONGEVITY ss2218716626 Dec 20, 2016 (150)
69 SYSTEMSBIOZJU ss2629083151 Nov 08, 2017 (151)
70 ILLUMINA ss2633425976 Nov 08, 2017 (151)
71 GRF ss2702228690 Nov 08, 2017 (151)
72 ILLUMINA ss2710857851 Nov 08, 2017 (151)
73 GNOMAD ss2952592932 Nov 08, 2017 (151)
74 SWEGEN ss3015922300 Nov 08, 2017 (151)
75 ILLUMINA ss3021806441 Nov 08, 2017 (151)
76 BIOINF_KMB_FNS_UNIBA ss3028410784 Nov 08, 2017 (151)
77 CSHL ss3351845203 Nov 08, 2017 (151)
78 ILLUMINA ss3625718621 Oct 12, 2018 (152)
79 ILLUMINA ss3627725453 Oct 12, 2018 (152)
80 ILLUMINA ss3631405313 Oct 12, 2018 (152)
81 ILLUMINA ss3633149368 Oct 12, 2018 (152)
82 ILLUMINA ss3633857412 Oct 12, 2018 (152)
83 ILLUMINA ss3634688302 Oct 12, 2018 (152)
84 ILLUMINA ss3635545002 Oct 12, 2018 (152)
85 ILLUMINA ss3636377108 Oct 12, 2018 (152)
86 ILLUMINA ss3637296563 Oct 12, 2018 (152)
87 ILLUMINA ss3638175758 Oct 12, 2018 (152)
88 ILLUMINA ss3639095888 Oct 12, 2018 (152)
89 ILLUMINA ss3639856083 Oct 12, 2018 (152)
90 ILLUMINA ss3640395612 Oct 12, 2018 (152)
91 ILLUMINA ss3641084325 Oct 12, 2018 (152)
92 ILLUMINA ss3641379821 Oct 12, 2018 (152)
93 ILLUMINA ss3643153049 Oct 12, 2018 (152)
94 ILLUMINA ss3643905399 Oct 12, 2018 (152)
95 ILLUMINA ss3644696453 Oct 12, 2018 (152)
96 URBANLAB ss3650704722 Oct 12, 2018 (152)
97 ILLUMINA ss3652224808 Oct 12, 2018 (152)
98 EGCUT_WGS ss3682786339 Jul 13, 2019 (153)
99 EVA_DECODE ss3700936545 Jul 13, 2019 (153)
100 ILLUMINA ss3725644762 Jul 13, 2019 (153)
101 ACPOP ss3742225818 Jul 13, 2019 (153)
102 ILLUMINA ss3744153450 Jul 13, 2019 (153)
103 ILLUMINA ss3744988546 Jul 13, 2019 (153)
104 EVA ss3754946428 Jul 13, 2019 (153)
105 PAGE_CC ss3771946635 Jul 13, 2019 (153)
106 ILLUMINA ss3772486197 Jul 13, 2019 (153)
107 PACBIO ss3788271163 Jul 13, 2019 (153)
108 PACBIO ss3793216133 Jul 13, 2019 (153)
109 PACBIO ss3798102139 Jul 13, 2019 (153)
110 KHV_HUMAN_GENOMES ss3820211412 Jul 13, 2019 (153)
111 EVA ss3834983216 Apr 27, 2020 (154)
112 EVA ss3841103623 Apr 27, 2020 (154)
113 EVA ss3846601932 Apr 27, 2020 (154)
114 HGDP ss3847571083 Apr 27, 2020 (154)
115 SGDP_PRJ ss3886239022 Apr 27, 2020 (154)
116 KRGDB ss3936017135 Apr 27, 2020 (154)
117 KOGIC ss3979315279 Apr 27, 2020 (154)
118 EVA ss3984726973 Apr 26, 2021 (155)
119 EVA ss3985804162 Apr 26, 2021 (155)
120 EVA ss4017779283 Apr 26, 2021 (155)
121 TOPMED ss5044210986 Apr 26, 2021 (155)
122 TOMMO_GENOMICS ss5223530456 Apr 26, 2021 (155)
123 1000G_HIGH_COVERAGE ss5303973668 Oct 16, 2022 (156)
124 EVA ss5315903417 Oct 16, 2022 (156)
125 EVA ss5429102397 Oct 16, 2022 (156)
126 HUGCELL_USP ss5496934708 Oct 16, 2022 (156)
127 EVA ss5511831103 Oct 16, 2022 (156)
128 1000G_HIGH_COVERAGE ss5608091652 Oct 16, 2022 (156)
129 SANFORD_IMAGENETICS ss5660563268 Oct 16, 2022 (156)
130 TOMMO_GENOMICS ss5780092639 Oct 16, 2022 (156)
131 EVA ss5799982186 Oct 16, 2022 (156)
132 YY_MCH ss5816737114 Oct 16, 2022 (156)
133 EVA ss5834303418 Oct 16, 2022 (156)
134 EVA ss5847808317 Oct 16, 2022 (156)
135 EVA ss5851900394 Oct 16, 2022 (156)
136 EVA ss5914871254 Oct 16, 2022 (156)
137 EVA ss5951966785 Oct 16, 2022 (156)
138 1000Genomes NC_000017.10 - 74551968 Oct 12, 2018 (152)
139 1000Genomes_30x NC_000017.11 - 76555886 Oct 16, 2022 (156)
140 The Avon Longitudinal Study of Parents and Children NC_000017.10 - 74551968 Oct 12, 2018 (152)
141 Genetic variation in the Estonian population NC_000017.10 - 74551968 Oct 12, 2018 (152)
142 The Danish reference pan genome NC_000017.10 - 74551968 Apr 27, 2020 (154)
143 gnomAD - Genomes NC_000017.11 - 76555886 Apr 26, 2021 (155)
144 Genome of the Netherlands Release 5 NC_000017.10 - 74551968 Apr 27, 2020 (154)
145 HGDP-CEPH-db Supplement 1 NC_000017.9 - 72063563 Apr 27, 2020 (154)
146 HapMap NC_000017.11 - 76555886 Apr 27, 2020 (154)
147 KOREAN population from KRGDB NC_000017.10 - 74551968 Apr 27, 2020 (154)
148 Korean Genome Project NC_000017.11 - 76555886 Apr 27, 2020 (154)
149 Northern Sweden NC_000017.10 - 74551968 Jul 13, 2019 (153)
150 The PAGE Study NC_000017.11 - 76555886 Jul 13, 2019 (153)
151 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000017.10 - 74551968 Apr 26, 2021 (155)
152 CNV burdens in cranial meningiomas NC_000017.10 - 74551968 Apr 26, 2021 (155)
153 Qatari NC_000017.10 - 74551968 Apr 27, 2020 (154)
154 SGDP_PRJ NC_000017.10 - 74551968 Apr 27, 2020 (154)
155 Siberian NC_000017.10 - 74551968 Apr 27, 2020 (154)
156 8.3KJPN NC_000017.10 - 74551968 Apr 26, 2021 (155)
157 14KJPN NC_000017.11 - 76555886 Oct 16, 2022 (156)
158 TopMed NC_000017.11 - 76555886 Apr 26, 2021 (155)
159 UK 10K study - Twins NC_000017.10 - 74551968 Oct 12, 2018 (152)
160 A Vietnamese Genetic Variation Database NC_000017.10 - 74551968 Jul 13, 2019 (153)
161 ALFA NC_000017.11 - 76555886 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)
rs56425261 May 24, 2008 (130)
rs58069445 May 24, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
43194529, ss3936017135 NC_000017.10:74551967:C:A NC_000017.11:76555885:C:A (self)
43194529, ss3936017135 NC_000017.10:74551967:C:G NC_000017.11:76555885:C:G (self)
248975, ss76738131, ss77543308, ss83488624, ss90663695, ss109928038, ss113851436, ss168513417, ss170252008, ss171742660, ss207910679, ss255799201, ss282845878, ss287217395, ss291996101, ss481510913, ss1697396261, ss1713599149, ss3639095888, ss3639856083, ss3643153049, ss3643905399, ss3847571083 NC_000017.9:72063562:C:T NC_000017.11:76555885:C:T (self)
72865045, 40377370, 28524587, 4447049, 17987361, 43194529, 15510683, 1030089, 276521, 18850515, 38256002, 10178817, 81499763, 40377370, 8923914, ss227662602, ss237325700, ss243603792, ss481539431, ss482514767, ss485550474, ss537452178, ss565413450, ss661227032, ss783220796, ss784175243, ss832481025, ss833099671, ss834054466, ss993345206, ss1081223287, ss1359587050, ss1428100192, ss1578248545, ss1636128727, ss1679122760, ss1752240995, ss1808885932, ss1936808593, ss1946473862, ss1959771495, ss1968437469, ss2029176291, ss2157662463, ss2629083151, ss2633425976, ss2702228690, ss2710857851, ss2952592932, ss3015922300, ss3021806441, ss3351845203, ss3625718621, ss3627725453, ss3631405313, ss3633149368, ss3633857412, ss3634688302, ss3635545002, ss3636377108, ss3637296563, ss3638175758, ss3640395612, ss3641084325, ss3641379821, ss3644696453, ss3652224808, ss3682786339, ss3742225818, ss3744153450, ss3744988546, ss3754946428, ss3772486197, ss3788271163, ss3793216133, ss3798102139, ss3834983216, ss3841103623, ss3886239022, ss3936017135, ss3984726973, ss3985804162, ss4017779283, ss5223530456, ss5315903417, ss5429102397, ss5511831103, ss5660563268, ss5799982186, ss5834303418, ss5847808317, ss5951966785 NC_000017.10:74551967:C:T NC_000017.11:76555885:C:T (self)
95617587, 514193543, 1529119, 35693280, 1168104, 113929743, 259756648, 6897632365, ss2218716626, ss3028410784, ss3650704722, ss3700936545, ss3725644762, ss3771946635, ss3820211412, ss3846601932, ss3979315279, ss5044210986, ss5303973668, ss5496934708, ss5608091652, ss5780092639, ss5816737114, ss5851900394, ss5914871254 NC_000017.11:76555885:C:T NC_000017.11:76555885:C:T (self)
ss10869078 NT_010641.13:8443725:C:T NC_000017.11:76555885:C:T (self)
ss14277620, ss16745774, ss20037853, ss21372551 NT_010641.14:8444128:C:T NC_000017.11:76555885:C:T (self)
ss40761401, ss67557655, ss67934236, ss68273225, ss70917082, ss71516028, ss75749370, ss84640197, ss106520883, ss136505664, ss137189502, ss154413550, ss154651171, ss159588636, ss160861800, ss174296069 NT_010783.15:39826119:C:T NC_000017.11:76555885: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 rs7219690

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