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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.

rs2913

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr22:18994584 (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
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.383936 (101624/264690, TOPMED)
G=0.373734 (52266/139848, GnomAD)
G=0.36869 (25040/67916, ALFA) (+ 20 more)
A=0.49338 (13942/28258, 14KJPN)
A=0.49445 (8287/16760, 8.3KJPN)
G=0.4760 (3048/6404, 1000G_30x)
G=0.4804 (2406/5008, 1000G)
G=0.3319 (1487/4480, Estonian)
G=0.3373 (1300/3854, ALSPAC)
G=0.3263 (1210/3708, TWINSUK)
G=0.4331 (1269/2930, KOREAN)
G=0.4391 (915/2084, HGDP_Stanford)
G=0.4482 (848/1892, HapMap)
G=0.4460 (817/1832, Korea1K)
G=0.295 (294/998, GoNL)
G=0.345 (207/600, NorthernSweden)
A=0.077 (41/534, MGP)
G=0.285 (113/396, SGDP_PRJ)
G=0.426 (92/216, Qatari)
G=0.379 (81/214, Vietnamese)
G=0.33 (22/66, Ancient Sardinia)
G=0.27 (12/44, Siberian)
G=0.28 (11/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
DGCR5 : Non Coding Transcript 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 67916 G=0.36869 A=0.63131
European Sub 54342 G=0.33757 A=0.66243
African Sub 4664 G=0.4168 A=0.5832
African Others Sub 176 G=0.438 A=0.562
African American Sub 4488 G=0.4160 A=0.5840
Asian Sub 192 G=0.458 A=0.542
East Asian Sub 150 G=0.420 A=0.580
Other Asian Sub 42 G=0.60 A=0.40
Latin American 1 Sub 250 G=0.396 A=0.604
Latin American 2 Sub 1242 G=0.4058 A=0.5942
South Asian Sub 4970 G=0.6260 A=0.3740
Other Sub 2256 G=0.4211 A=0.5789


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 G=0.383936 A=0.616064
gnomAD - Genomes Global Study-wide 139848 G=0.373734 A=0.626266
gnomAD - Genomes European Sub 75802 G=0.34101 A=0.65899
gnomAD - Genomes African Sub 41860 G=0.42076 A=0.57924
gnomAD - Genomes American Sub 13608 G=0.38235 A=0.61765
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=0.4488 A=0.5512
gnomAD - Genomes East Asian Sub 3112 G=0.4071 A=0.5929
gnomAD - Genomes Other Sub 2144 G=0.3932 A=0.6068
Allele Frequency Aggregator Total Global 67916 G=0.36869 A=0.63131
Allele Frequency Aggregator European Sub 54342 G=0.33757 A=0.66243
Allele Frequency Aggregator South Asian Sub 4970 G=0.6260 A=0.3740
Allele Frequency Aggregator African Sub 4664 G=0.4168 A=0.5832
Allele Frequency Aggregator Other Sub 2256 G=0.4211 A=0.5789
Allele Frequency Aggregator Latin American 2 Sub 1242 G=0.4058 A=0.5942
Allele Frequency Aggregator Latin American 1 Sub 250 G=0.396 A=0.604
Allele Frequency Aggregator Asian Sub 192 G=0.458 A=0.542
14KJPN JAPANESE Study-wide 28258 G=0.50662 A=0.49338
8.3KJPN JAPANESE Study-wide 16760 G=0.50555 A=0.49445
1000Genomes_30x Global Study-wide 6404 G=0.4760 A=0.5240
1000Genomes_30x African Sub 1786 G=0.4496 A=0.5504
1000Genomes_30x Europe Sub 1266 G=0.3199 A=0.6801
1000Genomes_30x South Asian Sub 1202 G=0.7280 A=0.2720
1000Genomes_30x East Asian Sub 1170 G=0.4368 A=0.5632
1000Genomes_30x American Sub 980 G=0.463 A=0.537
1000Genomes Global Study-wide 5008 G=0.4804 A=0.5196
1000Genomes African Sub 1322 G=0.4554 A=0.5446
1000Genomes East Asian Sub 1008 G=0.4435 A=0.5565
1000Genomes Europe Sub 1006 G=0.3231 A=0.6769
1000Genomes South Asian Sub 978 G=0.732 A=0.268
1000Genomes American Sub 694 G=0.455 A=0.545
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.3319 A=0.6681
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.3373 A=0.6627
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.3263 A=0.6737
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.4331 A=0.5669
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.4391 A=0.5609
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.445 A=0.555
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.543 A=0.457
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.417 A=0.583
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.312 A=0.688
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.496 A=0.504
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.292 A=0.708
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.72 A=0.28
HapMap Global Study-wide 1892 G=0.4482 A=0.5518
HapMap American Sub 770 G=0.483 A=0.517
HapMap African Sub 692 G=0.448 A=0.552
HapMap Asian Sub 254 G=0.457 A=0.543
HapMap Europe Sub 176 G=0.284 A=0.716
Korean Genome Project KOREAN Study-wide 1832 G=0.4460 A=0.5540
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.295 A=0.705
Northern Sweden ACPOP Study-wide 600 G=0.345 A=0.655
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 G=0.923 A=0.077
SGDP_PRJ Global Study-wide 396 G=0.285 A=0.715
Qatari Global Study-wide 216 G=0.426 A=0.574
A Vietnamese Genetic Variation Database Global Study-wide 214 G=0.379 A=0.621
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 66 G=0.33 A=0.67
Siberian Global Study-wide 44 G=0.27 A=0.73
The Danish reference pan genome Danish Study-wide 40 G=0.28 A=0.72
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 22 NC_000022.11:g.18994584G>A
GRCh37.p13 chr 22 NC_000022.10:g.18982097G>A
Gene: DGCR5, DiGeorge syndrome critical region gene 5 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
DGCR5 transcript variant 2 NR_045121.2:n.3164G>A N/A Non Coding Transcript Variant
DGCR5 transcript variant 1 NR_002733.3:n.3308G>A N/A Non Coding Transcript Variant
DGCR5 transcript variant 4 NR_024159.2:n. N/A Intron Variant
DGCR5 transcript variant 5 NR_026651.2:n. N/A Intron Variant
DGCR5 transcript variant 3 NR_110533.2:n. N/A Intron 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 G= A
GRCh38.p14 chr 22 NC_000022.11:g.18994584= NC_000022.11:g.18994584G>A
GRCh37.p13 chr 22 NC_000022.10:g.18982097= NC_000022.10:g.18982097G>A
DGCR5 transcript variant 1 NR_002733.3:n.3308= NR_002733.3:n.3308G>A
DGCR5 transcript variant 1 NR_002733.2:n.3278= NR_002733.2:n.3278G>A
DGCR5 transcript variant 2 NR_045121.2:n.3164= NR_045121.2:n.3164G>A
DGCR5 transcript variant 2 NR_045121.1:n.3134= NR_045121.1:n.3134G>A
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#.

124 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 WIAF ss2944 Sep 19, 2000 (36)
2 LEE ss1538552 Oct 05, 2000 (92)
3 KWOK ss1750167 Oct 18, 2000 (87)
4 SC_JCM ss3530233 Sep 28, 2001 (100)
5 LEE ss4398326 May 29, 2002 (106)
6 LEE ss4426164 May 29, 2002 (106)
7 WI_SSAHASNP ss12522589 Jul 11, 2003 (116)
8 SC_SNP ss13344122 Dec 05, 2003 (119)
9 CSHL-HAPMAP ss17720152 Feb 27, 2004 (120)
10 CSHL-HAPMAP ss19500489 Feb 27, 2004 (120)
11 SSAHASNP ss21852010 Apr 05, 2004 (121)
12 PERLEGEN ss23788127 Sep 20, 2004 (123)
13 SEQUENOM ss24797173 Sep 20, 2004 (123)
14 KRIBB_YJKIM ss65824225 Nov 29, 2006 (127)
15 ILLUMINA ss66809018 Nov 29, 2006 (127)
16 ILLUMINA ss67282869 Nov 29, 2006 (127)
17 ILLUMINA ss67685206 Nov 29, 2006 (127)
18 ILLUMINA ss70761387 May 25, 2008 (130)
19 ILLUMINA ss71335277 May 16, 2007 (127)
20 ILLUMINA ss75848892 Dec 06, 2007 (129)
21 HGSV ss78189720 Dec 06, 2007 (129)
22 ILLUMINA ss79153638 Dec 15, 2007 (130)
23 KRIBB_YJKIM ss83345561 Dec 15, 2007 (130)
24 BCMHGSC_JDW ss91875746 Mar 24, 2008 (129)
25 HUMANGENOME_JCVI ss96092329 Feb 05, 2009 (130)
26 BGI ss103840669 Dec 01, 2009 (131)
27 1000GENOMES ss112545553 Jan 25, 2009 (130)
28 1000GENOMES ss114025285 Jan 25, 2009 (130)
29 ILLUMINA-UK ss117359694 Feb 14, 2009 (130)
30 ILLUMINA ss122142219 Dec 01, 2009 (131)
31 ENSEMBL ss138334234 Dec 01, 2009 (131)
32 ENSEMBL ss143577265 Dec 01, 2009 (131)
33 ILLUMINA ss154245816 Dec 01, 2009 (131)
34 GMI ss157025126 Dec 01, 2009 (131)
35 ILLUMINA ss159422694 Dec 01, 2009 (131)
36 COMPLETE_GENOMICS ss167667378 Jul 04, 2010 (132)
37 COMPLETE_GENOMICS ss168869149 Jul 04, 2010 (132)
38 ILLUMINA ss171479549 Jul 04, 2010 (132)
39 COMPLETE_GENOMICS ss171824372 Jul 04, 2010 (132)
40 ILLUMINA ss173531776 Jul 04, 2010 (132)
41 BUSHMAN ss204047965 Jul 04, 2010 (132)
42 BCM-HGSC-SUB ss208817641 Jul 04, 2010 (132)
43 1000GENOMES ss228614481 Jul 14, 2010 (132)
44 1000GENOMES ss238019497 Jul 15, 2010 (132)
45 1000GENOMES ss244149232 Jul 15, 2010 (132)
46 BL ss255839583 May 09, 2011 (134)
47 GMI ss283584430 May 04, 2012 (137)
48 GMI ss287549429 Apr 25, 2013 (138)
49 PJP ss292734954 May 09, 2011 (134)
50 ILLUMINA ss479841421 May 04, 2012 (137)
51 ILLUMINA ss484287924 May 04, 2012 (137)
52 ILLUMINA ss533325430 Sep 08, 2015 (146)
53 TISHKOFF ss566555634 Apr 25, 2013 (138)
54 SSMP ss662478273 Apr 25, 2013 (138)
55 ILLUMINA ss779483073 Sep 08, 2015 (146)
56 ILLUMINA ss781081993 Sep 08, 2015 (146)
57 ILLUMINA ss825484156 Apr 01, 2015 (144)
58 ILLUMINA ss832934333 Jul 13, 2019 (153)
59 ILLUMINA ss834953114 Sep 08, 2015 (146)
60 EVA-GONL ss995214665 Aug 21, 2014 (142)
61 JMKIDD_LAB ss1082564852 Aug 21, 2014 (142)
62 1000GENOMES ss1366653152 Aug 21, 2014 (142)
63 DDI ss1429217635 Apr 01, 2015 (144)
64 EVA_GENOME_DK ss1579701116 Apr 01, 2015 (144)
65 EVA_UK10K_ALSPAC ss1639738296 Apr 01, 2015 (144)
66 EVA_UK10K_TWINSUK ss1682732329 Apr 01, 2015 (144)
67 EVA_DECODE ss1699283739 Apr 01, 2015 (144)
68 EVA_MGP ss1711559949 Apr 01, 2015 (144)
69 EVA_SVP ss1713730595 Apr 01, 2015 (144)
70 HAMMER_LAB ss1809730522 Sep 08, 2015 (146)
71 WEILL_CORNELL_DGM ss1938776169 Feb 12, 2016 (147)
72 GENOMED ss1969245395 Jul 19, 2016 (147)
73 JJLAB ss2030160828 Sep 14, 2016 (149)
74 USC_VALOUEV ss2158770399 Dec 20, 2016 (150)
75 HUMAN_LONGEVITY ss2246396941 Dec 20, 2016 (150)
76 SYSTEMSBIOZJU ss2629578480 Nov 08, 2017 (151)
77 ILLUMINA ss2633861798 Nov 08, 2017 (151)
78 GRF ss2704512820 Nov 08, 2017 (151)
79 GNOMAD ss2972902005 Nov 08, 2017 (151)
80 SWEGEN ss3019073259 Nov 08, 2017 (151)
81 BIOINF_KMB_FNS_UNIBA ss3028918280 Nov 08, 2017 (151)
82 CSHL ss3352772583 Nov 08, 2017 (151)
83 ILLUMINA ss3628504137 Oct 12, 2018 (152)
84 ILLUMINA ss3631814291 Oct 12, 2018 (152)
85 ILLUMINA ss3638373822 Oct 12, 2018 (152)
86 ILLUMINA ss3639190834 Oct 12, 2018 (152)
87 ILLUMINA ss3639611531 Oct 12, 2018 (152)
88 ILLUMINA ss3643334265 Oct 12, 2018 (152)
89 OMUKHERJEE_ADBS ss3646560975 Oct 12, 2018 (152)
90 URBANLAB ss3651150581 Oct 12, 2018 (152)
91 EGCUT_WGS ss3685606309 Jul 13, 2019 (153)
92 EVA_DECODE ss3707939539 Jul 13, 2019 (153)
93 ACPOP ss3743816320 Jul 13, 2019 (153)
94 EVA ss3759220907 Jul 13, 2019 (153)
95 PACBIO ss3788791197 Jul 13, 2019 (153)
96 PACBIO ss3793662603 Jul 13, 2019 (153)
97 PACBIO ss3798548921 Jul 13, 2019 (153)
98 KHV_HUMAN_GENOMES ss3822389538 Jul 13, 2019 (153)
99 EVA ss3835923640 Apr 27, 2020 (154)
100 EVA ss3841590521 Apr 27, 2020 (154)
101 EVA ss3847105132 Apr 27, 2020 (154)
102 HGDP ss3847684437 Apr 27, 2020 (154)
103 SGDP_PRJ ss3890240868 Apr 27, 2020 (154)
104 KRGDB ss3940621359 Apr 27, 2020 (154)
105 KOGIC ss3983372652 Apr 27, 2020 (154)
106 FSA-LAB ss3984229413 Apr 27, 2021 (155)
107 EVA ss3985909697 Apr 27, 2021 (155)
108 EVA ss3986086633 Apr 27, 2021 (155)
109 EVA ss4017873128 Apr 27, 2021 (155)
110 TOPMED ss5104853539 Apr 27, 2021 (155)
111 TOMMO_GENOMICS ss5232005583 Apr 27, 2021 (155)
112 1000G_HIGH_COVERAGE ss5310631574 Oct 16, 2022 (156)
113 EVA ss5316046329 Oct 16, 2022 (156)
114 EVA ss5440477178 Oct 16, 2022 (156)
115 HUGCELL_USP ss5502545656 Oct 16, 2022 (156)
116 1000G_HIGH_COVERAGE ss5617978676 Oct 16, 2022 (156)
117 SANFORD_IMAGENETICS ss5664221426 Oct 16, 2022 (156)
118 TOMMO_GENOMICS ss5792945324 Oct 16, 2022 (156)
119 YY_MCH ss5818588650 Oct 16, 2022 (156)
120 EVA ss5821889263 Oct 16, 2022 (156)
121 EVA ss5853342957 Oct 16, 2022 (156)
122 EVA ss5881318451 Oct 16, 2022 (156)
123 EVA ss5959092907 Oct 16, 2022 (156)
124 EVA ss5981123135 Oct 16, 2022 (156)
125 1000Genomes NC_000022.10 - 18982097 Oct 12, 2018 (152)
126 1000Genomes_30x NC_000022.11 - 18994584 Oct 16, 2022 (156)
127 The Avon Longitudinal Study of Parents and Children NC_000022.10 - 18982097 Oct 12, 2018 (152)
128 Genetic variation in the Estonian population NC_000022.10 - 18982097 Oct 12, 2018 (152)
129 The Danish reference pan genome NC_000022.10 - 18982097 Apr 27, 2020 (154)
130 gnomAD - Genomes NC_000022.11 - 18994584 Apr 27, 2021 (155)
131 Genome of the Netherlands Release 5 NC_000022.10 - 18982097 Apr 27, 2020 (154)
132 HGDP-CEPH-db Supplement 1 NC_000022.9 - 17362097 Apr 27, 2020 (154)
133 HapMap NC_000022.11 - 18994584 Apr 27, 2020 (154)
134 KOREAN population from KRGDB NC_000022.10 - 18982097 Apr 27, 2020 (154)
135 Korean Genome Project NC_000022.11 - 18994584 Apr 27, 2020 (154)
136 Medical Genome Project healthy controls from Spanish population NC_000022.10 - 18982097 Apr 27, 2020 (154)
137 Northern Sweden NC_000022.10 - 18982097 Jul 13, 2019 (153)
138 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000022.10 - 18982097 Apr 27, 2021 (155)
139 Qatari NC_000022.10 - 18982097 Apr 27, 2020 (154)
140 SGDP_PRJ NC_000022.10 - 18982097 Apr 27, 2020 (154)
141 Siberian NC_000022.10 - 18982097 Apr 27, 2020 (154)
142 8.3KJPN NC_000022.10 - 18982097 Apr 27, 2021 (155)
143 14KJPN NC_000022.11 - 18994584 Oct 16, 2022 (156)
144 TopMed NC_000022.11 - 18994584 Apr 27, 2021 (155)
145 UK 10K study - Twins NC_000022.10 - 18982097 Oct 12, 2018 (152)
146 A Vietnamese Genetic Variation Database NC_000022.10 - 18982097 Jul 13, 2019 (153)
147 ALFA NC_000022.11 - 18994584 Apr 27, 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)
rs1057717 Jan 18, 2001 (92)
rs3171561 Jul 03, 2002 (106)
rs59304651 May 25, 2008 (130)
rs386429648 Aug 21, 2014 (142)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss78189720, ss3639190834, ss3639611531 NC_000022.8:17356650:G:A NC_000022.11:18994583:G:A (self)
362329, ss91875746, ss112545553, ss114025285, ss117359694, ss167667378, ss168869149, ss171824372, ss204047965, ss208817641, ss255839583, ss283584430, ss287549429, ss292734954, ss484287924, ss825484156, ss1699283739, ss1713730595, ss3643334265, ss3847684437 NC_000022.9:17362096:G:A NC_000022.11:18994583:G:A (self)
80186544, 44364831, 31344557, 5866055, 19766203, 47798753, 675709, 17101185, 1135624, 20818091, 42257848, 11286753, 89974890, 44364831, 9788603, ss228614481, ss238019497, ss244149232, ss479841421, ss533325430, ss566555634, ss662478273, ss779483073, ss781081993, ss832934333, ss834953114, ss995214665, ss1082564852, ss1366653152, ss1429217635, ss1579701116, ss1639738296, ss1682732329, ss1711559949, ss1809730522, ss1938776169, ss1969245395, ss2030160828, ss2158770399, ss2629578480, ss2633861798, ss2704512820, ss2972902005, ss3019073259, ss3352772583, ss3628504137, ss3631814291, ss3638373822, ss3646560975, ss3685606309, ss3743816320, ss3759220907, ss3788791197, ss3793662603, ss3798548921, ss3835923640, ss3841590521, ss3890240868, ss3940621359, ss3984229413, ss3985909697, ss3986086633, ss4017873128, ss5232005583, ss5316046329, ss5440477178, ss5664221426, ss5821889263, ss5959092907, ss5981123135 NC_000022.10:18982096:G:A NC_000022.11:18994583:G:A (self)
105504611, 566333469, 2226240, 39750653, 126782428, 379962486, 16454000633, ss2246396941, ss3028918280, ss3651150581, ss3707939539, ss3822389538, ss3847105132, ss3983372652, ss5104853539, ss5310631574, ss5502545656, ss5617978676, ss5792945324, ss5818588650, ss5853342957, ss5881318451 NC_000022.11:18994583:G:A NC_000022.11:18994583:G:A (self)
ss2944, ss1538552, ss1750167, ss3530233, ss4398326, ss4426164, ss12522589, ss13344122, ss17720152, ss19500489, ss21852010, ss23788127, ss24797173, ss65824225, ss66809018, ss67282869, ss67685206, ss70761387, ss71335277, ss75848892, ss79153638, ss83345561, ss96092329, ss103840669, ss122142219, ss138334234, ss143577265, ss154245816, ss157025126, ss159422694, ss171479549, ss173531776 NT_011519.10:2134246:G:A NC_000022.11:18994583:G:A (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 rs2913

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