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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.

rs13122273

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr4:13100727 (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 / G>C / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.156776 (41497/264690, TOPMED)
T=0.200971 (46102/229396, ALFA)
T=0.157634 (22093/140154, GnomAD) (+ 20 more)
T=0.12610 (9924/78700, PAGE_STUDY)
T=0.19927 (5631/28258, 14KJPN)
T=0.20006 (3353/16760, 8.3KJPN)
T=0.1816 (1163/6404, 1000G_30x)
T=0.1865 (934/5008, 1000G)
T=0.2357 (1056/4480, Estonian)
T=0.2200 (848/3854, ALSPAC)
T=0.2163 (802/3708, TWINSUK)
T=0.2280 (668/2930, KOREAN)
T=0.2799 (318/1136, Daghestan)
T=0.252 (251/998, GoNL)
T=0.301 (237/788, PRJEB37584)
T=0.183 (110/600, NorthernSweden)
T=0.148 (49/330, HapMap)
G=0.422 (92/218, SGDP_PRJ)
T=0.162 (35/216, Qatari)
T=0.285 (61/214, Vietnamese)
T=0.33 (13/40, GENOME_DK)
G=0.40 (12/30, Siberian)
T=0.23 (6/26, Ancient Sardinia)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
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 234526 G=0.799724 A=0.000000, C=0.000000, T=0.200276
European Sub 207512 G=0.790465 A=0.000000, C=0.000000, T=0.209535
African Sub 10418 G=0.96832 A=0.00000, C=0.00000, T=0.03168
African Others Sub 400 G=0.990 A=0.000, C=0.000, T=0.010
African American Sub 10018 G=0.96746 A=0.00000, C=0.00000, T=0.03254
Asian Sub 3774 G=0.7621 A=0.0000, C=0.0000, T=0.2379
East Asian Sub 3050 G=0.7584 A=0.0000, C=0.0000, T=0.2416
Other Asian Sub 724 G=0.778 A=0.000, C=0.000, T=0.222
Latin American 1 Sub 934 G=0.840 A=0.000, C=0.000, T=0.160
Latin American 2 Sub 2328 G=0.8531 A=0.0000, C=0.0000, T=0.1469
South Asian Sub 320 G=0.647 A=0.000, C=0.000, T=0.353
Other Sub 9240 G=0.8207 A=0.0000, C=0.0000, T=0.1793


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=0.843224 T=0.156776
Allele Frequency Aggregator Total Global 229396 G=0.799029 A=0.000000, C=0.000000, T=0.200971
Allele Frequency Aggregator European Sub 204342 G=0.790479 A=0.000000, C=0.000000, T=0.209521
Allele Frequency Aggregator African Sub 9276 G=0.9702 A=0.0000, C=0.0000, T=0.0298
Allele Frequency Aggregator Other Sub 8422 G=0.8207 A=0.0000, C=0.0000, T=0.1793
Allele Frequency Aggregator Asian Sub 3774 G=0.7621 A=0.0000, C=0.0000, T=0.2379
Allele Frequency Aggregator Latin American 2 Sub 2328 G=0.8531 A=0.0000, C=0.0000, T=0.1469
Allele Frequency Aggregator Latin American 1 Sub 934 G=0.840 A=0.000, C=0.000, T=0.160
Allele Frequency Aggregator South Asian Sub 320 G=0.647 A=0.000, C=0.000, T=0.353
gnomAD - Genomes Global Study-wide 140154 G=0.842366 T=0.157634
gnomAD - Genomes European Sub 75880 G=0.78108 T=0.21892
gnomAD - Genomes African Sub 42032 G=0.95565 T=0.04435
gnomAD - Genomes American Sub 13652 G=0.85379 T=0.14621
gnomAD - Genomes Ashkenazi Jewish Sub 3316 G=0.8652 T=0.1348
gnomAD - Genomes East Asian Sub 3124 G=0.7343 T=0.2657
gnomAD - Genomes Other Sub 2150 G=0.8400 T=0.1600
The PAGE Study Global Study-wide 78700 G=0.87390 T=0.12610
The PAGE Study AfricanAmerican Sub 32516 G=0.95110 T=0.04890
The PAGE Study Mexican Sub 10810 G=0.83321 T=0.16679
The PAGE Study Asian Sub 8318 G=0.7965 T=0.2035
The PAGE Study PuertoRican Sub 7918 G=0.8784 T=0.1216
The PAGE Study NativeHawaiian Sub 4532 G=0.6589 T=0.3411
The PAGE Study Cuban Sub 4230 G=0.8310 T=0.1690
The PAGE Study Dominican Sub 3828 G=0.8989 T=0.1011
The PAGE Study CentralAmerican Sub 2450 G=0.8559 T=0.1441
The PAGE Study SouthAmerican Sub 1982 G=0.8396 T=0.1604
The PAGE Study NativeAmerican Sub 1260 G=0.8325 T=0.1675
The PAGE Study SouthAsian Sub 856 G=0.597 T=0.403
14KJPN JAPANESE Study-wide 28258 G=0.80073 T=0.19927
8.3KJPN JAPANESE Study-wide 16760 G=0.79994 T=0.20006
1000Genomes_30x Global Study-wide 6404 G=0.8184 T=0.1816
1000Genomes_30x African Sub 1786 G=0.9849 T=0.0151
1000Genomes_30x Europe Sub 1266 G=0.8017 T=0.1983
1000Genomes_30x South Asian Sub 1202 G=0.6406 T=0.3594
1000Genomes_30x East Asian Sub 1170 G=0.7444 T=0.2556
1000Genomes_30x American Sub 980 G=0.843 T=0.157
1000Genomes Global Study-wide 5008 G=0.8135 T=0.1865
1000Genomes African Sub 1322 G=0.9849 T=0.0151
1000Genomes East Asian Sub 1008 G=0.7540 T=0.2460
1000Genomes Europe Sub 1006 G=0.8032 T=0.1968
1000Genomes South Asian Sub 978 G=0.636 T=0.364
1000Genomes American Sub 694 G=0.839 T=0.161
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.7643 T=0.2357
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.7800 T=0.2200
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.7837 T=0.2163
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.7720 T=0.2280
Genome-wide autozygosity in Daghestan Global Study-wide 1136 G=0.7201 T=0.2799
Genome-wide autozygosity in Daghestan Daghestan Sub 628 G=0.713 T=0.287
Genome-wide autozygosity in Daghestan Near_East Sub 144 G=0.799 T=0.201
Genome-wide autozygosity in Daghestan Central Asia Sub 122 G=0.639 T=0.361
Genome-wide autozygosity in Daghestan Europe Sub 108 G=0.806 T=0.194
Genome-wide autozygosity in Daghestan South Asian Sub 98 G=0.63 T=0.37
Genome-wide autozygosity in Daghestan Caucasus Sub 36 G=0.78 T=0.22
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.748 T=0.252
CNV burdens in cranial meningiomas Global Study-wide 788 G=0.699 T=0.301
CNV burdens in cranial meningiomas CRM Sub 788 G=0.699 T=0.301
Northern Sweden ACPOP Study-wide 600 G=0.817 T=0.183
HapMap Global Study-wide 330 G=0.852 T=0.148
HapMap African Sub 120 G=1.000 T=0.000
HapMap American Sub 120 G=0.775 T=0.225
HapMap Asian Sub 90 G=0.76 T=0.24
SGDP_PRJ Global Study-wide 218 G=0.422 T=0.578
Qatari Global Study-wide 216 G=0.838 T=0.162
A Vietnamese Genetic Variation Database Global Study-wide 214 G=0.715 T=0.285
The Danish reference pan genome Danish Study-wide 40 G=0.68 T=0.33
Siberian Global Study-wide 30 G=0.40 T=0.60
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 26 G=0.77 T=0.23
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 4 NC_000004.12:g.13100727G>A
GRCh38.p14 chr 4 NC_000004.12:g.13100727G>C
GRCh38.p14 chr 4 NC_000004.12:g.13100727G>T
GRCh37.p13 chr 4 NC_000004.11:g.13102351G>A
GRCh37.p13 chr 4 NC_000004.11:g.13102351G>C
GRCh37.p13 chr 4 NC_000004.11:g.13102351G>T
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 C T
GRCh38.p14 chr 4 NC_000004.12:g.13100727= NC_000004.12:g.13100727G>A NC_000004.12:g.13100727G>C NC_000004.12:g.13100727G>T
GRCh37.p13 chr 4 NC_000004.11:g.13102351= NC_000004.11:g.13102351G>A NC_000004.11:g.13102351G>C NC_000004.11:g.13102351G>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#.

103 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 SSAHASNP ss22110037 Apr 05, 2004 (121)
2 ABI ss44499755 Mar 15, 2006 (126)
3 PERLEGEN ss68891209 May 18, 2007 (127)
4 HUMANGENOME_JCVI ss98934645 Feb 05, 2009 (130)
5 1000GENOMES ss112931553 Jan 25, 2009 (130)
6 ENSEMBL ss135147060 Dec 01, 2009 (131)
7 ILLUMINA ss160318313 Dec 01, 2009 (131)
8 COMPLETE_GENOMICS ss161923137 Jul 04, 2010 (132)
9 COMPLETE_GENOMICS ss166176633 Jul 04, 2010 (132)
10 1000GENOMES ss232267366 Jul 14, 2010 (132)
11 1000GENOMES ss239586891 Jul 15, 2010 (132)
12 BL ss252944891 May 09, 2011 (134)
13 GMI ss277582909 May 04, 2012 (137)
14 GMI ss284850102 Apr 25, 2013 (138)
15 PJP ss293213306 May 09, 2011 (134)
16 ILLUMINA ss479873668 May 04, 2012 (137)
17 ILLUMINA ss479881377 May 04, 2012 (137)
18 ILLUMINA ss480490016 Sep 08, 2015 (146)
19 ILLUMINA ss484735276 May 04, 2012 (137)
20 ILLUMINA ss536833057 Sep 08, 2015 (146)
21 SSMP ss651087523 Apr 25, 2013 (138)
22 ILLUMINA ss778421397 Sep 08, 2015 (146)
23 ILLUMINA ss782814334 Sep 08, 2015 (146)
24 ILLUMINA ss783779522 Sep 08, 2015 (146)
25 ILLUMINA ss832067582 Sep 08, 2015 (146)
26 ILLUMINA ss833876762 Sep 08, 2015 (146)
27 EVA-GONL ss979786818 Aug 21, 2014 (142)
28 JMKIDD_LAB ss1071291005 Aug 21, 2014 (142)
29 1000GENOMES ss1308515192 Aug 21, 2014 (142)
30 HAMMER_LAB ss1397367241 Sep 08, 2015 (146)
31 DDI ss1429780587 Apr 01, 2015 (144)
32 EVA_GENOME_DK ss1580423337 Apr 01, 2015 (144)
33 EVA_DECODE ss1589274909 Apr 01, 2015 (144)
34 EVA_UK10K_ALSPAC ss1609449120 Apr 01, 2015 (144)
35 EVA_UK10K_TWINSUK ss1652443153 Apr 01, 2015 (144)
36 ILLUMINA ss1752497850 Sep 08, 2015 (146)
37 WEILL_CORNELL_DGM ss1923026761 Feb 12, 2016 (147)
38 ILLUMINA ss1946110487 Feb 12, 2016 (147)
39 ILLUMINA ss1958662328 Feb 12, 2016 (147)
40 GENOMED ss1969663341 Sep 14, 2016 (149)
41 JJLAB ss2022084555 Sep 14, 2016 (149)
42 USC_VALOUEV ss2150196022 Dec 20, 2016 (150)
43 HUMAN_LONGEVITY ss2260564726 Dec 20, 2016 (150)
44 SYSTEMSBIOZJU ss2625544301 Nov 08, 2017 (151)
45 ILLUMINA ss2634084267 Nov 08, 2017 (151)
46 ILLUMINA ss2634084268 Nov 08, 2017 (151)
47 GRF ss2705639632 Nov 08, 2017 (151)
48 GNOMAD ss2805862156 Nov 08, 2017 (151)
49 AFFY ss2985286375 Nov 08, 2017 (151)
50 AFFY ss2985909323 Nov 08, 2017 (151)
51 SWEGEN ss2994174727 Nov 08, 2017 (151)
52 ILLUMINA ss3022349229 Nov 08, 2017 (151)
53 BIOINF_KMB_FNS_UNIBA ss3024811681 Nov 08, 2017 (151)
54 CSHL ss3345554722 Nov 08, 2017 (151)
55 ILLUMINA ss3625838053 Oct 12, 2018 (152)
56 ILLUMINA ss3628905746 Oct 12, 2018 (152)
57 ILLUMINA ss3632022785 Oct 12, 2018 (152)
58 ILLUMINA ss3633326282 Oct 12, 2018 (152)
59 ILLUMINA ss3634044974 Oct 12, 2018 (152)
60 ILLUMINA ss3634941714 Oct 12, 2018 (152)
61 ILLUMINA ss3635728094 Oct 12, 2018 (152)
62 ILLUMINA ss3636643076 Oct 12, 2018 (152)
63 ILLUMINA ss3637480589 Oct 12, 2018 (152)
64 ILLUMINA ss3640649010 Oct 12, 2018 (152)
65 ILLUMINA ss3644843195 Oct 12, 2018 (152)
66 URBANLAB ss3647656864 Oct 12, 2018 (152)
67 ILLUMINA ss3652832199 Oct 12, 2018 (152)
68 ILLUMINA ss3654056869 Oct 12, 2018 (152)
69 EGCUT_WGS ss3662080975 Jul 13, 2019 (153)
70 EVA_DECODE ss3711447662 Jul 13, 2019 (153)
71 ILLUMINA ss3726111295 Jul 13, 2019 (153)
72 ACPOP ss3730873759 Jul 13, 2019 (153)
73 ILLUMINA ss3744230518 Jul 13, 2019 (153)
74 ILLUMINA ss3745242013 Jul 13, 2019 (153)
75 EVA ss3761423905 Jul 13, 2019 (153)
76 PAGE_CC ss3771107055 Jul 13, 2019 (153)
77 ILLUMINA ss3772736704 Jul 13, 2019 (153)
78 KHV_HUMAN_GENOMES ss3804558769 Jul 13, 2019 (153)
79 EVA ss3828381273 Apr 26, 2020 (154)
80 EVA ss3837623726 Apr 26, 2020 (154)
81 EVA ss3843057830 Apr 26, 2020 (154)
82 SGDP_PRJ ss3858267335 Apr 26, 2020 (154)
83 KRGDB ss3904413499 Apr 26, 2020 (154)
84 EVA ss3984523877 Apr 26, 2021 (155)
85 EVA ss3985053475 Apr 26, 2021 (155)
86 TOPMED ss4603522572 Apr 26, 2021 (155)
87 TOMMO_GENOMICS ss5164297296 Apr 26, 2021 (155)
88 1000G_HIGH_COVERAGE ss5258119619 Oct 13, 2022 (156)
89 EVA ss5314936857 Oct 13, 2022 (156)
90 EVA ss5347038073 Oct 13, 2022 (156)
91 HUGCELL_USP ss5457011289 Oct 13, 2022 (156)
92 EVA ss5507395731 Oct 13, 2022 (156)
93 1000G_HIGH_COVERAGE ss5538592963 Oct 13, 2022 (156)
94 SANFORD_IMAGENETICS ss5624547951 Oct 13, 2022 (156)
95 SANFORD_IMAGENETICS ss5634393343 Oct 13, 2022 (156)
96 TOMMO_GENOMICS ss5697973069 Oct 13, 2022 (156)
97 EVA ss5799607778 Oct 13, 2022 (156)
98 YY_MCH ss5804777252 Oct 13, 2022 (156)
99 EVA ss5843580956 Oct 13, 2022 (156)
100 EVA ss5848002195 Oct 13, 2022 (156)
101 EVA ss5854088249 Oct 13, 2022 (156)
102 EVA ss5862228463 Oct 13, 2022 (156)
103 EVA ss5962769037 Oct 13, 2022 (156)
104 1000Genomes NC_000004.11 - 13102351 Oct 12, 2018 (152)
105 1000Genomes_30x NC_000004.12 - 13100727 Oct 13, 2022 (156)
106 The Avon Longitudinal Study of Parents and Children NC_000004.11 - 13102351 Oct 12, 2018 (152)
107 Genome-wide autozygosity in Daghestan NC_000004.10 - 12711449 Apr 26, 2020 (154)
108 Genetic variation in the Estonian population NC_000004.11 - 13102351 Oct 12, 2018 (152)
109 The Danish reference pan genome NC_000004.11 - 13102351 Apr 26, 2020 (154)
110 gnomAD - Genomes NC_000004.12 - 13100727 Apr 26, 2021 (155)
111 Genome of the Netherlands Release 5 NC_000004.11 - 13102351 Apr 26, 2020 (154)
112 HapMap NC_000004.12 - 13100727 Apr 26, 2020 (154)
113 KOREAN population from KRGDB NC_000004.11 - 13102351 Apr 26, 2020 (154)
114 Northern Sweden NC_000004.11 - 13102351 Jul 13, 2019 (153)
115 The PAGE Study NC_000004.12 - 13100727 Jul 13, 2019 (153)
116 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000004.11 - 13102351 Apr 26, 2021 (155)
117 CNV burdens in cranial meningiomas NC_000004.11 - 13102351 Apr 26, 2021 (155)
118 Qatari NC_000004.11 - 13102351 Apr 26, 2020 (154)
119 SGDP_PRJ NC_000004.11 - 13102351 Apr 26, 2020 (154)
120 Siberian NC_000004.11 - 13102351 Apr 26, 2020 (154)
121 8.3KJPN NC_000004.11 - 13102351 Apr 26, 2021 (155)
122 14KJPN NC_000004.12 - 13100727 Oct 13, 2022 (156)
123 TopMed NC_000004.12 - 13100727 Apr 26, 2021 (155)
124 UK 10K study - Twins NC_000004.11 - 13102351 Oct 12, 2018 (152)
125 A Vietnamese Genetic Variation Database NC_000004.11 - 13102351 Jul 13, 2019 (153)
126 ALFA NC_000004.12 - 13100727 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).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss2805862156 NC_000004.11:13102350:G:A NC_000004.12:13100726:G:A (self)
13036412490, ss2260564726, ss5804777252 NC_000004.12:13100726:G:A NC_000004.12:13100726:G:A (self)
13036412490 NC_000004.12:13100726:G:C NC_000004.12:13100726:G:C (self)
342878, ss112931553, ss161923137, ss166176633, ss252944891, ss277582909, ss284850102, ss293213306, ss479873668, ss1397367241, ss1589274909 NC_000004.10:12711448:G:T NC_000004.12:13100726:G:T (self)
19865690, 11059931, 7819223, 6588276, 4867121, 11590893, 4158624, 279402, 73236, 5068691, 10284315, 2712376, 22266603, 11059931, 2417281, ss232267366, ss239586891, ss479881377, ss480490016, ss484735276, ss536833057, ss651087523, ss778421397, ss782814334, ss783779522, ss832067582, ss833876762, ss979786818, ss1071291005, ss1308515192, ss1429780587, ss1580423337, ss1609449120, ss1652443153, ss1752497850, ss1923026761, ss1946110487, ss1958662328, ss1969663341, ss2022084555, ss2150196022, ss2625544301, ss2634084267, ss2634084268, ss2705639632, ss2805862156, ss2985286375, ss2985909323, ss2994174727, ss3022349229, ss3345554722, ss3625838053, ss3628905746, ss3632022785, ss3633326282, ss3634044974, ss3634941714, ss3635728094, ss3636643076, ss3637480589, ss3640649010, ss3644843195, ss3652832199, ss3654056869, ss3662080975, ss3730873759, ss3744230518, ss3745242013, ss3761423905, ss3772736704, ss3828381273, ss3837623726, ss3858267335, ss3904413499, ss3984523877, ss3985053475, ss5164297296, ss5314936857, ss5347038073, ss5507395731, ss5624547951, ss5634393343, ss5799607778, ss5843580956, ss5848002195, ss5962769037 NC_000004.11:13102350:G:T NC_000004.12:13100726:G:T (self)
26118898, 140816885, 2559720, 328524, 31810173, 440900128, 13036412490, ss2260564726, ss3024811681, ss3647656864, ss3711447662, ss3726111295, ss3771107055, ss3804558769, ss3843057830, ss4603522572, ss5258119619, ss5457011289, ss5538592963, ss5697973069, ss5804777252, ss5854088249, ss5862228463 NC_000004.12:13100726:G:T NC_000004.12:13100726:G:T (self)
ss22110037 NT_006316.15:3777708:G:T NC_000004.12:13100726:G:T (self)
ss44499755, ss68891209, ss98934645, ss135147060, ss160318313 NT_006316.16:4284147:G:T NC_000004.12:13100726:G:T (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 rs13122273
PMID Title Author Year Journal
22228203 A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network. Aslibekyan S et al. 2012 Pharmacogenetics and genomics
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