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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.

rs1314

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr22:24526484 (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
T>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.161362 (42711/264690, TOPMED)
G=0.180278 (34656/192236, ALFA)
G=0.162000 (22692/140074, GnomAD) (+ 19 more)
G=0.10047 (2839/28258, 14KJPN)
G=0.10089 (1691/16760, 8.3KJPN)
G=0.1594 (1021/6404, 1000G_30x)
G=0.1599 (801/5008, 1000G)
G=0.1688 (756/4480, Estonian)
G=0.1692 (652/3854, ALSPAC)
G=0.1772 (657/3708, TWINSUK)
G=0.1000 (293/2930, KOREAN)
G=0.1464 (305/2084, HGDP_Stanford)
G=0.1386 (262/1890, HapMap)
G=0.0955 (175/1832, Korea1K)
G=0.196 (196/998, GoNL)
G=0.158 (95/600, NorthernSweden)
G=0.250 (54/216, Qatari)
G=0.079 (17/216, Vietnamese)
T=0.449 (80/178, SGDP_PRJ)
G=0.14 (14/100, Ancient Sardinia)
G=0.17 (7/40, GENOME_DK)
T=0.33 (4/12, Siberian)
Clinical Significance
Reported in ClinVar
Gene : Consequence
UPB1 : 3 Prime UTR 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 192236 T=0.819722 G=0.180278
European Sub 165102 T=0.818785 G=0.181215
African Sub 7064 T=0.8773 G=0.1227
African Others Sub 264 T=0.852 G=0.148
African American Sub 6800 T=0.8782 G=0.1218
Asian Sub 700 T=0.910 G=0.090
East Asian Sub 554 T=0.919 G=0.081
Other Asian Sub 146 T=0.877 G=0.123
Latin American 1 Sub 840 T=0.843 G=0.157
Latin American 2 Sub 6886 T=0.8164 G=0.1836
South Asian Sub 5040 T=0.7486 G=0.2514
Other Sub 6604 T=0.8268 G=0.1732


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 T=0.838638 G=0.161362
Allele Frequency Aggregator Total Global 192236 T=0.819722 G=0.180278
Allele Frequency Aggregator European Sub 165102 T=0.818785 G=0.181215
Allele Frequency Aggregator African Sub 7064 T=0.8773 G=0.1227
Allele Frequency Aggregator Latin American 2 Sub 6886 T=0.8164 G=0.1836
Allele Frequency Aggregator Other Sub 6604 T=0.8268 G=0.1732
Allele Frequency Aggregator South Asian Sub 5040 T=0.7486 G=0.2514
Allele Frequency Aggregator Latin American 1 Sub 840 T=0.843 G=0.157
Allele Frequency Aggregator Asian Sub 700 T=0.910 G=0.090
gnomAD - Genomes Global Study-wide 140074 T=0.838000 G=0.162000
gnomAD - Genomes European Sub 75856 T=0.82725 G=0.17275
gnomAD - Genomes African Sub 41982 T=0.86985 G=0.13015
gnomAD - Genomes American Sub 13644 T=0.79771 G=0.20229
gnomAD - Genomes Ashkenazi Jewish Sub 3312 T=0.7660 G=0.2340
gnomAD - Genomes East Asian Sub 3130 T=0.9319 G=0.0681
gnomAD - Genomes Other Sub 2150 T=0.8251 G=0.1749
14KJPN JAPANESE Study-wide 28258 T=0.89953 G=0.10047
8.3KJPN JAPANESE Study-wide 16760 T=0.89911 G=0.10089
1000Genomes_30x Global Study-wide 6404 T=0.8406 G=0.1594
1000Genomes_30x African Sub 1786 T=0.8746 G=0.1254
1000Genomes_30x Europe Sub 1266 T=0.8468 G=0.1532
1000Genomes_30x South Asian Sub 1202 T=0.7238 G=0.2762
1000Genomes_30x East Asian Sub 1170 T=0.9342 G=0.0658
1000Genomes_30x American Sub 980 T=0.802 G=0.198
1000Genomes Global Study-wide 5008 T=0.8401 G=0.1599
1000Genomes African Sub 1322 T=0.8707 G=0.1293
1000Genomes East Asian Sub 1008 T=0.9325 G=0.0675
1000Genomes Europe Sub 1006 T=0.8459 G=0.1541
1000Genomes South Asian Sub 978 T=0.726 G=0.274
1000Genomes American Sub 694 T=0.800 G=0.200
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.8313 G=0.1688
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.8308 G=0.1692
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.8228 G=0.1772
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.9000 G=0.1000
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 T=0.8536 G=0.1464
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 T=0.932 G=0.068
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 T=0.761 G=0.239
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 T=0.820 G=0.180
HGDP-CEPH-db Supplement 1 Europe Sub 320 T=0.847 G=0.153
HGDP-CEPH-db Supplement 1 Africa Sub 242 T=0.905 G=0.095
HGDP-CEPH-db Supplement 1 America Sub 216 T=0.907 G=0.093
HGDP-CEPH-db Supplement 1 Oceania Sub 72 T=0.74 G=0.26
HapMap Global Study-wide 1890 T=0.8614 G=0.1386
HapMap American Sub 770 T=0.835 G=0.165
HapMap African Sub 690 T=0.878 G=0.122
HapMap Asian Sub 254 T=0.902 G=0.098
HapMap Europe Sub 176 T=0.852 G=0.148
Korean Genome Project KOREAN Study-wide 1832 T=0.9045 G=0.0955
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.804 G=0.196
Northern Sweden ACPOP Study-wide 600 T=0.842 G=0.158
Qatari Global Study-wide 216 T=0.750 G=0.250
A Vietnamese Genetic Variation Database Global Study-wide 216 T=0.921 G=0.079
SGDP_PRJ Global Study-wide 178 T=0.449 G=0.551
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 100 T=0.86 G=0.14
The Danish reference pan genome Danish Study-wide 40 T=0.82 G=0.17
Siberian Global Study-wide 12 T=0.33 G=0.67
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.24526484T>G
GRCh37.p13 chr 22 NC_000022.10:g.24922452T>G
UPB1 RefSeqGene NG_012858.2:g.36202T>G
Gene: UPB1, beta-ureidopropionase 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
UPB1 transcript NM_016327.3:c.*690= N/A 3 Prime UTR Variant
UPB1 transcript variant X2 XM_011530223.3:c. N/A Genic Downstream Transcript Variant
UPB1 transcript variant X1 XM_047441404.1:c. N/A Genic Downstream Transcript Variant
UPB1 transcript variant X4 XM_047441405.1:c. N/A Genic Downstream Transcript Variant
UPB1 transcript variant X3 XR_001755249.2:n. N/A Genic Downstream 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.

Allele: G (allele ID: 352236 )
ClinVar Accession Disease Names Clinical Significance
RCV000301290.3 Deficiency of beta-ureidopropionase Benign
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 T= G
GRCh38.p14 chr 22 NC_000022.11:g.24526484= NC_000022.11:g.24526484T>G
GRCh37.p13 chr 22 NC_000022.10:g.24922452= NC_000022.10:g.24922452T>G
UPB1 RefSeqGene NG_012858.2:g.36202= NG_012858.2:g.36202T>G
UPB1 transcript NM_016327.3:c.*690= NM_016327.3:c.*690T>G
UPB1 transcript NM_016327.2:c.*690= NM_016327.2:c.*690T>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#.

119 SubSNP, 22 Frequency, 1 ClinVar submissions
No Submitter Submission ID Date (Build)
1 WIAF ss1339 Sep 19, 2000 (36)
2 LEE ss1535222 Oct 04, 2000 (86)
3 CGAP-GAI ss4322867 Jan 04, 2002 (102)
4 SC_SNP ss8291191 Apr 21, 2003 (114)
5 CGAP-GAI ss16224000 Feb 27, 2004 (120)
6 CSHL-HAPMAP ss16925185 Feb 27, 2004 (120)
7 PERLEGEN ss23611860 Sep 20, 2004 (123)
8 ABI ss44310978 Mar 13, 2006 (126)
9 SI_EXO ss52071161 Oct 16, 2006 (127)
10 ILLUMINA ss65740726 Oct 16, 2006 (127)
11 KRIBB_YJKIM ss65824221 Dec 01, 2006 (127)
12 ILLUMINA ss66828875 Dec 01, 2006 (127)
13 ILLUMINA ss67059816 Dec 01, 2006 (127)
14 ILLUMINA ss67387303 Dec 01, 2006 (127)
15 ILLUMINA ss70419677 May 17, 2007 (127)
16 ILLUMINA ss70595328 May 26, 2008 (130)
17 ILLUMINA ss71139658 May 17, 2007 (127)
18 ILLUMINA ss75922877 Dec 07, 2007 (129)
19 KRIBB_YJKIM ss83344573 Dec 15, 2007 (130)
20 BCMHGSC_JDW ss91892106 Mar 24, 2008 (129)
21 1000GENOMES ss114078828 Jan 25, 2009 (130)
22 ILLUMINA ss121622042 Dec 01, 2009 (131)
23 ENSEMBL ss138340912 Dec 01, 2009 (131)
24 ILLUMINA ss153322374 Dec 01, 2009 (131)
25 ILLUMINA ss159246262 Dec 01, 2009 (131)
26 ILLUMINA ss160319225 Dec 01, 2009 (131)
27 COMPLETE_GENOMICS ss168980502 Jul 04, 2010 (132)
28 ILLUMINA ss170298814 Jul 04, 2010 (132)
29 ILLUMINA ss172335673 Jul 04, 2010 (132)
30 BUSHMAN ss204061007 Jul 04, 2010 (132)
31 1000GENOMES ss228635039 Jul 14, 2010 (132)
32 1000GENOMES ss238034792 Jul 15, 2010 (132)
33 1000GENOMES ss244161962 Jul 15, 2010 (132)
34 PJP ss292743249 May 09, 2011 (134)
35 ILLUMINA ss479876438 May 04, 2012 (137)
36 ILLUMINA ss479884156 May 04, 2012 (137)
37 ILLUMINA ss480493643 Sep 08, 2015 (146)
38 ILLUMINA ss484736664 May 04, 2012 (137)
39 ILLUMINA ss536834103 Sep 08, 2015 (146)
40 TISHKOFF ss566581828 Apr 25, 2013 (138)
41 SSMP ss662511119 Apr 25, 2013 (138)
42 ILLUMINA ss778796243 Sep 08, 2015 (146)
43 ILLUMINA ss782815025 Sep 08, 2015 (146)
44 ILLUMINA ss783780205 Sep 08, 2015 (146)
45 ILLUMINA ss825388951 Apr 01, 2015 (144)
46 ILLUMINA ss832068282 Sep 08, 2015 (146)
47 ILLUMINA ss832758552 Jul 13, 2019 (153)
48 ILLUMINA ss834256345 Sep 08, 2015 (146)
49 EVA-GONL ss995258499 Aug 21, 2014 (142)
50 JMKIDD_LAB ss1082593229 Aug 21, 2014 (142)
51 1000GENOMES ss1366823896 Aug 21, 2014 (142)
52 DDI ss1429231682 Apr 01, 2015 (144)
53 EVA_GENOME_DK ss1579717547 Apr 01, 2015 (144)
54 EVA_UK10K_ALSPAC ss1639814854 Apr 01, 2015 (144)
55 EVA_UK10K_TWINSUK ss1682808887 Apr 01, 2015 (144)
56 EVA_DECODE ss1699326670 Apr 01, 2015 (144)
57 EVA_SVP ss1713733682 Apr 01, 2015 (144)
58 ILLUMINA ss1752415675 Sep 08, 2015 (146)
59 HAMMER_LAB ss1809749507 Sep 08, 2015 (146)
60 WEILL_CORNELL_DGM ss1938824894 Feb 12, 2016 (147)
61 GENOMED ss1969254085 Jul 19, 2016 (147)
62 JJLAB ss2030184523 Sep 14, 2016 (149)
63 USC_VALOUEV ss2158797204 Dec 20, 2016 (150)
64 HUMAN_LONGEVITY ss2246655693 Dec 20, 2016 (150)
65 SYSTEMSBIOZJU ss2629590589 Nov 08, 2017 (151)
66 ILLUMINA ss2633866299 Nov 08, 2017 (151)
67 GRF ss2704545790 Nov 08, 2017 (151)
68 GNOMAD ss2973418233 Nov 08, 2017 (151)
69 SWEGEN ss3019160137 Nov 08, 2017 (151)
70 BIOINF_KMB_FNS_UNIBA ss3028929451 Nov 08, 2017 (151)
71 CSHL ss3352795995 Nov 08, 2017 (151)
72 ILLUMINA ss3625800404 Oct 12, 2018 (152)
73 ILLUMINA ss3628512733 Oct 12, 2018 (152)
74 ILLUMINA ss3631818262 Oct 12, 2018 (152)
75 ILLUMINA ss3633269771 Oct 12, 2018 (152)
76 ILLUMINA ss3633985332 Oct 12, 2018 (152)
77 ILLUMINA ss3634862651 Oct 12, 2018 (152)
78 ILLUMINA ss3635669865 Oct 12, 2018 (152)
79 ILLUMINA ss3636558513 Oct 12, 2018 (152)
80 ILLUMINA ss3637422089 Oct 12, 2018 (152)
81 ILLUMINA ss3638376809 Oct 12, 2018 (152)
82 ILLUMINA ss3639192018 Oct 12, 2018 (152)
83 ILLUMINA ss3639612221 Oct 12, 2018 (152)
84 ILLUMINA ss3640569951 Oct 12, 2018 (152)
85 ILLUMINA ss3643337012 Oct 12, 2018 (152)
86 EGCUT_WGS ss3685662239 Jul 13, 2019 (153)
87 EVA_DECODE ss3708022525 Jul 13, 2019 (153)
88 ACPOP ss3743854791 Jul 13, 2019 (153)
89 ILLUMINA ss3745162472 Jul 13, 2019 (153)
90 EVA ss3759274306 Jul 13, 2019 (153)
91 ILLUMINA ss3772658458 Jul 13, 2019 (153)
92 PACBIO ss3788804079 Jul 13, 2019 (153)
93 PACBIO ss3793673595 Jul 13, 2019 (153)
94 PACBIO ss3798560008 Jul 13, 2019 (153)
95 KHV_HUMAN_GENOMES ss3822440757 Jul 13, 2019 (153)
96 EVA ss3825967469 Apr 27, 2020 (154)
97 EVA ss3835944894 Apr 27, 2020 (154)
98 HGDP ss3847685769 Apr 27, 2020 (154)
99 SGDP_PRJ ss3890360599 Apr 27, 2020 (154)
100 KRGDB ss3940753010 Apr 27, 2020 (154)
101 KOGIC ss3983460040 Apr 27, 2020 (154)
102 EVA ss3985911880 Apr 27, 2021 (155)
103 EVA ss4017875467 Apr 27, 2021 (155)
104 TOPMED ss5106221985 Apr 27, 2021 (155)
105 TOMMO_GENOMICS ss5232226764 Apr 27, 2021 (155)
106 1000G_HIGH_COVERAGE ss5310793779 Oct 16, 2022 (156)
107 EVA ss5316049066 Oct 16, 2022 (156)
108 EVA ss5440754422 Oct 16, 2022 (156)
109 HUGCELL_USP ss5502667729 Oct 16, 2022 (156)
110 1000G_HIGH_COVERAGE ss5618211911 Oct 16, 2022 (156)
111 SANFORD_IMAGENETICS ss5664322835 Oct 16, 2022 (156)
112 TOMMO_GENOMICS ss5793222217 Oct 16, 2022 (156)
113 EVA ss5800038272 Oct 16, 2022 (156)
114 YY_MCH ss5818634505 Oct 16, 2022 (156)
115 EVA ss5821951006 Oct 16, 2022 (156)
116 EVA ss5853360754 Oct 16, 2022 (156)
117 EVA ss5881477201 Oct 16, 2022 (156)
118 EVA ss5959174211 Oct 16, 2022 (156)
119 EVA ss5981128233 Oct 16, 2022 (156)
120 1000Genomes NC_000022.10 - 24922452 Oct 12, 2018 (152)
121 1000Genomes_30x NC_000022.11 - 24526484 Oct 16, 2022 (156)
122 The Avon Longitudinal Study of Parents and Children NC_000022.10 - 24922452 Oct 12, 2018 (152)
123 Genetic variation in the Estonian population NC_000022.10 - 24922452 Oct 12, 2018 (152)
124 The Danish reference pan genome NC_000022.10 - 24922452 Apr 27, 2020 (154)
125 gnomAD - Genomes NC_000022.11 - 24526484 Apr 27, 2021 (155)
126 Genome of the Netherlands Release 5 NC_000022.10 - 24922452 Apr 27, 2020 (154)
127 HGDP-CEPH-db Supplement 1 NC_000022.9 - 23252452 Apr 27, 2020 (154)
128 HapMap NC_000022.11 - 24526484 Apr 27, 2020 (154)
129 KOREAN population from KRGDB NC_000022.10 - 24922452 Apr 27, 2020 (154)
130 Korean Genome Project NC_000022.11 - 24526484 Apr 27, 2020 (154)
131 Northern Sweden NC_000022.10 - 24922452 Jul 13, 2019 (153)
132 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000022.10 - 24922452 Apr 27, 2021 (155)
133 Qatari NC_000022.10 - 24922452 Apr 27, 2020 (154)
134 SGDP_PRJ NC_000022.10 - 24922452 Apr 27, 2020 (154)
135 Siberian NC_000022.10 - 24922452 Apr 27, 2020 (154)
136 8.3KJPN NC_000022.10 - 24922452 Apr 27, 2021 (155)
137 14KJPN NC_000022.11 - 24526484 Oct 16, 2022 (156)
138 TopMed NC_000022.11 - 24526484 Apr 27, 2021 (155)
139 UK 10K study - Twins NC_000022.10 - 24922452 Oct 12, 2018 (152)
140 A Vietnamese Genetic Variation Database NC_000022.10 - 24922452 Jul 13, 2019 (153)
141 ALFA NC_000022.11 - 24526484 Apr 27, 2021 (155)
142 ClinVar RCV000301290.3 Oct 16, 2022 (156)
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)
rs17401033 Oct 07, 2004 (123)
rs61006143 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss3639192018, ss3639612221 NC_000022.8:23247005:T:G NC_000022.11:24526483:T:G (self)
363661, ss91892106, ss114078828, ss168980502, ss204061007, ss292743249, ss479876438, ss825388951, ss1699326670, ss1713733682, ss3643337012, ss3847685769 NC_000022.9:23252451:T:G NC_000022.11:24526483:T:G (self)
80363166, 44449670, 31400487, 5882486, 19806414, 47930404, 17139656, 1137807, 20866816, 42377579, 11313558, 90196071, 44449670, 9808306, ss228635039, ss238034792, ss244161962, ss479884156, ss480493643, ss484736664, ss536834103, ss566581828, ss662511119, ss778796243, ss782815025, ss783780205, ss832068282, ss832758552, ss834256345, ss995258499, ss1082593229, ss1366823896, ss1429231682, ss1579717547, ss1639814854, ss1682808887, ss1752415675, ss1809749507, ss1938824894, ss1969254085, ss2030184523, ss2158797204, ss2629590589, ss2633866299, ss2704545790, ss2973418233, ss3019160137, ss3352795995, ss3625800404, ss3628512733, ss3631818262, ss3633269771, ss3633985332, ss3634862651, ss3635669865, ss3636558513, ss3637422089, ss3638376809, ss3640569951, ss3685662239, ss3743854791, ss3745162472, ss3759274306, ss3772658458, ss3788804079, ss3793673595, ss3798560008, ss3825967469, ss3835944894, ss3890360599, ss3940753010, ss3985911880, ss4017875467, ss5232226764, ss5316049066, ss5440754422, ss5664322835, ss5800038272, ss5821951006, ss5959174211, ss5981128233 NC_000022.10:24922451:T:G NC_000022.11:24526483:T:G (self)
RCV000301290.3, 105737846, 567507799, 2234423, 39838041, 127059321, 381330932, 8576320544, ss2246655693, ss3028929451, ss3708022525, ss3822440757, ss3983460040, ss5106221985, ss5310793779, ss5502667729, ss5618211911, ss5793222217, ss5818634505, ss5853360754, ss5881477201 NC_000022.11:24526483:T:G NC_000022.11:24526483:T:G (self)
ss16925185 NT_011520.9:4313020:T:G NC_000022.11:24526483:T:G (self)
ss52071161 NT_011520.10:4313020:T:G NC_000022.11:24526483:T:G (self)
ss1339, ss1535222, ss4322867, ss8291191, ss16224000, ss23611860, ss44310978, ss65740726, ss65824221, ss66828875, ss67059816, ss67387303, ss70419677, ss70595328, ss71139658, ss75922877, ss83344573, ss121622042, ss138340912, ss153322374, ss159246262, ss160319225, ss170298814, ss172335673 NT_011520.12:4313020:T:G NC_000022.11:24526483:T:G (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 rs1314

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