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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.

rs26531

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr5:115814828 (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>A / T>G
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.493007 (130494/264690, TOPMED)
G=0.489901 (68595/140018, GnomAD)
G=0.41874 (15924/38028, ALFA) (+ 18 more)
G=0.46790 (13222/28258, 14KJPN)
G=0.46527 (7798/16760, 8.3KJPN)
T=0.4892 (3133/6404, 1000G_30x)
T=0.4950 (2479/5008, 1000G)
G=0.3757 (1683/4480, Estonian)
G=0.3913 (1508/3854, ALSPAC)
G=0.3797 (1408/3708, TWINSUK)
G=0.4294 (1258/2930, KOREAN)
T=0.4630 (876/1892, HapMap)
G=0.4541 (832/1832, Korea1K)
T=0.4850 (549/1132, Daghestan)
G=0.382 (381/998, GoNL)
G=0.363 (218/600, NorthernSweden)
T=0.326 (126/386, SGDP_PRJ)
T=0.366 (79/216, Qatari)
G=0.259 (55/212, Vietnamese)
G=0.42 (17/40, GENOME_DK)
T=0.39 (15/38, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
CDO1 : Intron 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 38028 T=0.58126 A=0.00000, G=0.41874
European Sub 27308 T=0.63934 A=0.00000, G=0.36066
African Sub 5590 T=0.3730 A=0.0000, G=0.6270
African Others Sub 174 T=0.270 A=0.000, G=0.730
African American Sub 5416 T=0.3763 A=0.0000, G=0.6237
Asian Sub 132 T=0.795 A=0.000, G=0.205
East Asian Sub 82 T=0.84 A=0.00, G=0.16
Other Asian Sub 50 T=0.72 A=0.00, G=0.28
Latin American 1 Sub 210 T=0.533 A=0.000, G=0.467
Latin American 2 Sub 2412 T=0.4548 A=0.0000, G=0.5452
South Asian Sub 54 T=0.59 A=0.00, G=0.41
Other Sub 2322 T=0.5228 A=0.0000, G=0.4772


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=0.493007 G=0.506993
gnomAD - Genomes Global Study-wide 140018 T=0.510099 G=0.489901
gnomAD - Genomes European Sub 75848 T=0.60682 G=0.39318
gnomAD - Genomes African Sub 41942 T=0.34271 G=0.65729
gnomAD - Genomes American Sub 13632 T=0.46075 G=0.53925
gnomAD - Genomes Ashkenazi Jewish Sub 3324 T=0.4609 G=0.5391
gnomAD - Genomes East Asian Sub 3122 T=0.6867 G=0.3133
gnomAD - Genomes Other Sub 2150 T=0.4958 G=0.5042
Allele Frequency Aggregator Total Global 38028 T=0.58126 A=0.00000, G=0.41874
Allele Frequency Aggregator European Sub 27308 T=0.63934 A=0.00000, G=0.36066
Allele Frequency Aggregator African Sub 5590 T=0.3730 A=0.0000, G=0.6270
Allele Frequency Aggregator Latin American 2 Sub 2412 T=0.4548 A=0.0000, G=0.5452
Allele Frequency Aggregator Other Sub 2322 T=0.5228 A=0.0000, G=0.4772
Allele Frequency Aggregator Latin American 1 Sub 210 T=0.533 A=0.000, G=0.467
Allele Frequency Aggregator Asian Sub 132 T=0.795 A=0.000, G=0.205
Allele Frequency Aggregator South Asian Sub 54 T=0.59 A=0.00, G=0.41
14KJPN JAPANESE Study-wide 28258 T=0.53210 G=0.46790
8.3KJPN JAPANESE Study-wide 16760 T=0.53473 G=0.46527
1000Genomes_30x Global Study-wide 6404 T=0.4892 G=0.5108
1000Genomes_30x African Sub 1786 T=0.2945 G=0.7055
1000Genomes_30x Europe Sub 1266 T=0.5774 G=0.4226
1000Genomes_30x South Asian Sub 1202 T=0.5324 G=0.4676
1000Genomes_30x East Asian Sub 1170 T=0.6821 G=0.3179
1000Genomes_30x American Sub 980 T=0.447 G=0.553
1000Genomes Global Study-wide 5008 T=0.4950 G=0.5050
1000Genomes African Sub 1322 T=0.3011 G=0.6989
1000Genomes East Asian Sub 1008 T=0.6736 G=0.3264
1000Genomes Europe Sub 1006 T=0.5696 G=0.4304
1000Genomes South Asian Sub 978 T=0.528 G=0.472
1000Genomes American Sub 694 T=0.451 G=0.549
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.6243 G=0.3757
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.6087 G=0.3913
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.6203 G=0.3797
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.5706 G=0.4294
HapMap Global Study-wide 1892 T=0.4630 G=0.5370
HapMap American Sub 770 T=0.536 G=0.464
HapMap African Sub 692 T=0.329 G=0.671
HapMap Asian Sub 254 T=0.587 G=0.413
HapMap Europe Sub 176 T=0.489 G=0.511
Korean Genome Project KOREAN Study-wide 1832 T=0.5459 G=0.4541
Genome-wide autozygosity in Daghestan Global Study-wide 1132 T=0.4850 G=0.5150
Genome-wide autozygosity in Daghestan Daghestan Sub 628 T=0.462 G=0.538
Genome-wide autozygosity in Daghestan Near_East Sub 144 T=0.424 G=0.576
Genome-wide autozygosity in Daghestan Central Asia Sub 122 T=0.541 G=0.459
Genome-wide autozygosity in Daghestan Europe Sub 106 T=0.604 G=0.396
Genome-wide autozygosity in Daghestan South Asian Sub 96 T=0.55 G=0.45
Genome-wide autozygosity in Daghestan Caucasus Sub 36 T=0.42 G=0.58
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.618 G=0.382
Northern Sweden ACPOP Study-wide 600 T=0.637 G=0.363
SGDP_PRJ Global Study-wide 386 T=0.326 G=0.674
Qatari Global Study-wide 216 T=0.366 G=0.634
A Vietnamese Genetic Variation Database Global Study-wide 212 T=0.741 G=0.259
The Danish reference pan genome Danish Study-wide 40 T=0.57 G=0.42
Siberian Global Study-wide 38 T=0.39 G=0.61
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.115814828T>A
GRCh38.p14 chr 5 NC_000005.10:g.115814828T>G
GRCh37.p13 chr 5 NC_000005.9:g.115150525T>A
GRCh37.p13 chr 5 NC_000005.9:g.115150525T>G
Gene: CDO1, cysteine dioxygenase type 1 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
CDO1 transcript variant 1 NM_001323565.2:c.171-874A…

NM_001323565.2:c.171-874A>T

 		N/A Intron Variant
CDO1 transcript variant 3 NM_001323566.2:c.170+1400…

NM_001323566.2:c.170+1400A>T

 		N/A Intron Variant
CDO1 transcript variant 4 NM_001323567.2:c.-46-1570…

NM_001323567.2:c.-46-1570A>T

 		N/A Intron Variant
CDO1 transcript variant 2 NM_001801.3:c.170+1400A>T N/A Intron Variant
CDO1 transcript variant 5 NR_136618.2:n. N/A Intron Variant
CDO1 transcript variant 6 NR_136619.2:n. N/A Intron Variant
CDO1 transcript variant 7 NR_136620.2:n. N/A Intron Variant
CDO1 transcript variant 8 NR_136621.2:n. N/A Intron Variant
CDO1 transcript variant X2 XM_047416629.1:c.-103-874…

XM_047416629.1:c.-103-874A>T

 		N/A Intron Variant
CDO1 transcript variant X1 XM_047416628.1:c.-534= N/A 5 Prime UTR 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 T= A G
GRCh38.p14 chr 5 NC_000005.10:g.115814828= NC_000005.10:g.115814828T>A NC_000005.10:g.115814828T>G
GRCh37.p13 chr 5 NC_000005.9:g.115150525= NC_000005.9:g.115150525T>A NC_000005.9:g.115150525T>G
CDO1 transcript variant X1 XM_047416628.1:c.-534= XM_047416628.1:c.-534A>T XM_047416628.1:c.-534A>C
CDO1 transcript variant 1 NM_001323565.2:c.171-874= NM_001323565.2:c.171-874A>T NM_001323565.2:c.171-874A>C
CDO1 transcript variant 3 NM_001323566.2:c.170+1400= NM_001323566.2:c.170+1400A>T NM_001323566.2:c.170+1400A>C
CDO1 transcript variant 4 NM_001323567.2:c.-46-1570= NM_001323567.2:c.-46-1570A>T NM_001323567.2:c.-46-1570A>C
CDO1 transcript variant 2 NM_001801.2:c.170+1400= NM_001801.2:c.170+1400A>T NM_001801.2:c.170+1400A>C
CDO1 transcript variant 2 NM_001801.3:c.170+1400= NM_001801.3:c.170+1400A>T NM_001801.3:c.170+1400A>C
CDO1 transcript variant X2 XM_047416629.1:c.-103-874= XM_047416629.1:c.-103-874A>T XM_047416629.1:c.-103-874A>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#.

110 SubSNP, 21 Frequency submissions
No Submitter Submission ID Date (Build)
1 KWOK ss37923 May 08, 2000 (76)
2 KWOK ss37958 May 08, 2000 (76)
3 TSC-CSHL ss128076 Oct 05, 2000 (87)
4 KWOK ss322727 Jul 10, 2000 (79)
5 KWOK ss337669 Jul 10, 2000 (79)
6 SC_JCM ss500194 Jul 16, 2000 (87)
7 SC_JCM ss530213 Jul 16, 2000 (87)
8 KWOK ss969021 Oct 04, 2000 (87)
9 KWOK ss969696 Oct 04, 2000 (87)
10 KWOK ss971351 Oct 04, 2000 (87)
11 KWOK ss971729 Oct 04, 2000 (87)
12 KWOK ss1682109 Oct 18, 2000 (87)
13 KWOK ss1682280 Oct 18, 2000 (87)
14 WUGSC_SSAHASNP ss14452506 Dec 05, 2003 (119)
15 SC_SNP ss14815337 Dec 05, 2003 (119)
16 CSHL-HAPMAP ss17848328 Feb 27, 2004 (120)
17 CSHL-HAPMAP ss19630188 Feb 27, 2004 (120)
18 SSAHASNP ss22222906 Apr 05, 2004 (121)
19 ABI ss42440341 Mar 13, 2006 (126)
20 PERLEGEN ss46558719 Mar 13, 2006 (126)
21 AFFY ss66322917 Nov 29, 2006 (127)
22 PERLEGEN ss68946479 May 17, 2007 (127)
23 ILLUMINA ss74991104 Dec 06, 2007 (129)
24 AFFY ss76012997 Dec 06, 2007 (129)
25 KRIBB_YJKIM ss81404804 Dec 14, 2007 (130)
26 HUMANGENOME_JCVI ss98641694 Feb 04, 2009 (130)
27 BGI ss104230053 Dec 01, 2009 (131)
28 1000GENOMES ss109338499 Jan 24, 2009 (130)
29 1000GENOMES ss113103879 Jan 25, 2009 (130)
30 ILLUMINA-UK ss116771255 Feb 14, 2009 (130)
31 ENSEMBL ss139806969 Dec 01, 2009 (131)
32 GMI ss155915440 Dec 01, 2009 (131)
33 COMPLETE_GENOMICS ss162574494 Jul 04, 2010 (132)
34 COMPLETE_GENOMICS ss165753050 Jul 04, 2010 (132)
35 AFFY ss170406355 Jul 04, 2010 (132)
36 ILLUMINA ss173419495 Jul 04, 2010 (132)
37 BUSHMAN ss200724326 Jul 04, 2010 (132)
38 1000GENOMES ss221900702 Jul 14, 2010 (132)
39 1000GENOMES ss233103558 Jul 14, 2010 (132)
40 1000GENOMES ss240236533 Jul 15, 2010 (132)
41 GMI ss278440392 May 04, 2012 (137)
42 GMI ss285246143 Apr 25, 2013 (138)
43 PJP ss293440258 May 09, 2011 (134)
44 ILLUMINA ss483249821 May 04, 2012 (137)
45 ILLUMINA ss484913271 May 04, 2012 (137)
46 ILLUMINA ss535468021 Sep 08, 2015 (146)
47 TISHKOFF ss558641242 Apr 25, 2013 (138)
48 SSMP ss652532754 Apr 25, 2013 (138)
49 ILLUMINA ss780207043 Aug 21, 2014 (142)
50 ILLUMINA ss782068395 Aug 21, 2014 (142)
51 ILLUMINA ss835691781 Aug 21, 2014 (142)
52 EVA-GONL ss981999227 Aug 21, 2014 (142)
53 JMKIDD_LAB ss1072950172 Aug 21, 2014 (142)
54 1000GENOMES ss1316746323 Aug 21, 2014 (142)
55 HAMMER_LAB ss1397424372 Sep 08, 2015 (146)
56 DDI ss1430468099 Apr 01, 2015 (144)
57 EVA_GENOME_DK ss1581303141 Apr 01, 2015 (144)
58 EVA_DECODE ss1591521900 Apr 01, 2015 (144)
59 EVA_UK10K_ALSPAC ss1613761163 Apr 01, 2015 (144)
60 EVA_UK10K_TWINSUK ss1656755196 Apr 01, 2015 (144)
61 EVA_SVP ss1712792092 Apr 01, 2015 (144)
62 HAMMER_LAB ss1804029933 Sep 08, 2015 (146)
63 WEILL_CORNELL_DGM ss1925254500 Feb 12, 2016 (147)
64 GENOMED ss1970184673 Jul 19, 2016 (147)
65 JJLAB ss2023233509 Sep 14, 2016 (149)
66 USC_VALOUEV ss2151389700 Dec 20, 2016 (150)
67 HUMAN_LONGEVITY ss2277163525 Dec 20, 2016 (150)
68 SYSTEMSBIOZJU ss2626107853 Nov 08, 2017 (151)
69 ILLUMINA ss2634326119 Nov 08, 2017 (151)
70 GRF ss2706948617 Nov 08, 2017 (151)
71 GNOMAD ss2829431955 Nov 08, 2017 (151)
72 AFFY ss2985964890 Nov 08, 2017 (151)
73 SWEGEN ss2997605899 Nov 08, 2017 (151)
74 CSHL ss3346574457 Nov 08, 2017 (151)
75 ILLUMINA ss3629317309 Oct 12, 2018 (152)
76 ILLUMINA ss3632250851 Oct 12, 2018 (152)
77 ILLUMINA ss3638574447 Oct 12, 2018 (152)
78 ILLUMINA ss3642437901 Oct 12, 2018 (152)
79 ILLUMINA ss3643518907 Oct 12, 2018 (152)
80 BIOINF_KMB_FNS_UNIBA ss3645901368 Oct 12, 2018 (152)
81 URBANLAB ss3648146809 Oct 12, 2018 (152)
82 EGCUT_WGS ss3665508617 Jul 13, 2019 (153)
83 EVA_DECODE ss3715476596 Jul 13, 2019 (153)
84 ACPOP ss3732715341 Jul 13, 2019 (153)
85 EVA ss3763920705 Jul 13, 2019 (153)
86 PACBIO ss3785219458 Jul 13, 2019 (153)
87 PACBIO ss3790607992 Jul 13, 2019 (153)
88 PACBIO ss3795484774 Jul 13, 2019 (153)
89 KHV_HUMAN_GENOMES ss3807091458 Jul 13, 2019 (153)
90 EVA ss3829446774 Apr 26, 2020 (154)
91 EVA ss3838199158 Apr 26, 2020 (154)
92 EVA ss3843641277 Apr 26, 2020 (154)
93 SGDP_PRJ ss3862731609 Apr 26, 2020 (154)
94 KRGDB ss3909350306 Apr 26, 2020 (154)
95 KOGIC ss3957439309 Apr 26, 2020 (154)
96 EVA ss4017225739 Apr 26, 2021 (155)
97 TOPMED ss4674611850 Apr 26, 2021 (155)
98 TOMMO_GENOMICS ss5173620961 Apr 26, 2021 (155)
99 1000G_HIGH_COVERAGE ss5265429106 Oct 13, 2022 (156)
100 EVA ss5315078303 Oct 13, 2022 (156)
101 EVA ss5360216464 Oct 13, 2022 (156)
102 HUGCELL_USP ss5463441398 Oct 13, 2022 (156)
103 1000G_HIGH_COVERAGE ss5549863385 Oct 13, 2022 (156)
104 SANFORD_IMAGENETICS ss5638643313 Oct 13, 2022 (156)
105 TOMMO_GENOMICS ss5710549424 Oct 13, 2022 (156)
106 YY_MCH ss5806668946 Oct 13, 2022 (156)
107 EVA ss5835484578 Oct 13, 2022 (156)
108 EVA ss5854972939 Oct 13, 2022 (156)
109 EVA ss5895845931 Oct 13, 2022 (156)
110 EVA ss5967099072 Oct 13, 2022 (156)
111 1000Genomes NC_000005.9 - 115150525 Oct 12, 2018 (152)
112 1000Genomes_30x NC_000005.10 - 115814828 Oct 13, 2022 (156)
113 The Avon Longitudinal Study of Parents and Children NC_000005.9 - 115150525 Oct 12, 2018 (152)
114 Genome-wide autozygosity in Daghestan NC_000005.8 - 115178424 Apr 26, 2020 (154)
115 Genetic variation in the Estonian population NC_000005.9 - 115150525 Oct 12, 2018 (152)
116 The Danish reference pan genome NC_000005.9 - 115150525 Apr 26, 2020 (154)
117 gnomAD - Genomes NC_000005.10 - 115814828 Apr 26, 2021 (155)
118 Genome of the Netherlands Release 5 NC_000005.9 - 115150525 Apr 26, 2020 (154)
119 HapMap NC_000005.10 - 115814828 Apr 26, 2020 (154)
120 KOREAN population from KRGDB NC_000005.9 - 115150525 Apr 26, 2020 (154)
121 Korean Genome Project NC_000005.10 - 115814828 Apr 26, 2020 (154)
122 Northern Sweden NC_000005.9 - 115150525 Jul 13, 2019 (153)
123 Qatari NC_000005.9 - 115150525 Apr 26, 2020 (154)
124 SGDP_PRJ NC_000005.9 - 115150525 Apr 26, 2020 (154)
125 Siberian NC_000005.9 - 115150525 Apr 26, 2020 (154)
126 8.3KJPN NC_000005.9 - 115150525 Apr 26, 2021 (155)
127 14KJPN NC_000005.10 - 115814828 Oct 13, 2022 (156)
128 TopMed NC_000005.10 - 115814828 Apr 26, 2021 (155)
129 UK 10K study - Twins NC_000005.9 - 115150525 Oct 12, 2018 (152)
130 A Vietnamese Genetic Variation Database NC_000005.9 - 115150525 Jul 13, 2019 (153)
131 ALFA NC_000005.10 - 115814828 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)
rs120523 Oct 18, 2000 (87)
rs696535 Oct 18, 2000 (87)
rs756549 Oct 18, 2000 (87)
rs57032862 Feb 26, 2009 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
7596288607 NC_000005.10:115814827:T:A NC_000005.10:115814827:T:A (self)
399271, ss109338499, ss113103879, ss116771255, ss162574494, ss165753050, ss200724326, ss278440392, ss285246143, ss293440258, ss484913271, ss1397424372, ss1591521900, ss1712792092, ss3643518907 NC_000005.8:115178423:T:G NC_000005.10:115814827:T:G (self)
28408041, 15797920, 11246865, 7468080, 7021121, 16527700, 6000206, 7296430, 14748589, 3906054, 31590268, 15797920, 3505036, ss221900702, ss233103558, ss240236533, ss483249821, ss535468021, ss558641242, ss652532754, ss780207043, ss782068395, ss835691781, ss981999227, ss1072950172, ss1316746323, ss1430468099, ss1581303141, ss1613761163, ss1656755196, ss1804029933, ss1925254500, ss1970184673, ss2023233509, ss2151389700, ss2626107853, ss2634326119, ss2706948617, ss2829431955, ss2985964890, ss2997605899, ss3346574457, ss3629317309, ss3632250851, ss3638574447, ss3642437901, ss3665508617, ss3732715341, ss3763920705, ss3785219458, ss3790607992, ss3795484774, ss3829446774, ss3838199158, ss3862731609, ss3909350306, ss4017225739, ss5173620961, ss5315078303, ss5360216464, ss5638643313, ss5835484578, ss5967099072 NC_000005.9:115150524:T:G NC_000005.10:115814827:T:G (self)
37389320, 200952427, 2946191, 13817310, 44386528, 511989407, 7596288607, ss2277163525, ss3645901368, ss3648146809, ss3715476596, ss3807091458, ss3843641277, ss3957439309, ss4674611850, ss5265429106, ss5463441398, ss5549863385, ss5710549424, ss5806668946, ss5854972939, ss5895845931 NC_000005.10:115814827:T:G NC_000005.10:115814827:T:G (self)
ss14452506, ss14815337, ss17848328, ss19630188, ss22222906 NT_034772.5:17565537:T:G NC_000005.10:115814827:T:G (self)
ss37923, ss37958, ss128076, ss322727, ss337669, ss500194, ss530213, ss969021, ss969696, ss971351, ss971729, ss1682109, ss1682280, ss42440341, ss46558719, ss66322917, ss68946479, ss74991104, ss76012997, ss81404804, ss98641694, ss104230053, ss139806969, ss155915440, ss170406355, ss173419495 NT_034772.6:23464396:T:G NC_000005.10:115814827: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 rs26531

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