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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.

rs4382936

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr11:73241355 (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
A>C / A>T
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.366372 (96975/264690, TOPMED)
C=0.344855 (69069/200284, ALFA)
C=0.355949 (49867/140096, GnomAD) (+ 19 more)
A=0.26550 (7502/28256, 14KJPN)
A=0.26936 (4514/16758, 8.3KJPN)
C=0.4129 (2644/6404, 1000G_30x)
C=0.4171 (2089/5008, 1000G)
C=0.4031 (1806/4480, Estonian)
C=0.3516 (1355/3854, ALSPAC)
C=0.3465 (1285/3708, TWINSUK)
A=0.3259 (955/2930, KOREAN)
C=0.4712 (982/2084, HGDP_Stanford)
C=0.4143 (783/1890, HapMap)
A=0.3412 (625/1832, Korea1K)
C=0.334 (333/998, GoNL)
A=0.380 (300/790, PRJEB37584)
C=0.413 (248/600, NorthernSweden)
A=0.318 (124/390, SGDP_PRJ)
C=0.306 (66/216, Qatari)
C=0.32 (22/68, Ancient Sardinia)
C=0.42 (17/40, GENOME_DK)
A=0.24 (9/38, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
P2RY2 : 3 Prime UTR Variant
Publications
3 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 200284 A=0.655145 C=0.344855
European Sub 174490 A=0.657190 C=0.342810
African Sub 9718 A=0.7165 C=0.2835
African Others Sub 348 A=0.736 C=0.264
African American Sub 9370 A=0.7158 C=0.2842
Asian Sub 702 A=0.333 C=0.667
East Asian Sub 556 A=0.326 C=0.674
Other Asian Sub 146 A=0.363 C=0.637
Latin American 1 Sub 780 A=0.668 C=0.332
Latin American 2 Sub 2842 A=0.4258 C=0.5742
South Asian Sub 5042 A=0.6729 C=0.3271
Other Sub 6710 A=0.6291 C=0.3709


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 A=0.633628 C=0.366372
Allele Frequency Aggregator Total Global 200284 A=0.655145 C=0.344855
Allele Frequency Aggregator European Sub 174490 A=0.657190 C=0.342810
Allele Frequency Aggregator African Sub 9718 A=0.7165 C=0.2835
Allele Frequency Aggregator Other Sub 6710 A=0.6291 C=0.3709
Allele Frequency Aggregator South Asian Sub 5042 A=0.6729 C=0.3271
Allele Frequency Aggregator Latin American 2 Sub 2842 A=0.4258 C=0.5742
Allele Frequency Aggregator Latin American 1 Sub 780 A=0.668 C=0.332
Allele Frequency Aggregator Asian Sub 702 A=0.333 C=0.667
gnomAD - Genomes Global Study-wide 140096 A=0.644051 C=0.355949
gnomAD - Genomes European Sub 75858 A=0.63715 C=0.36285
gnomAD - Genomes African Sub 41994 A=0.71760 C=0.28240
gnomAD - Genomes American Sub 13640 A=0.50513 C=0.49487
gnomAD - Genomes Ashkenazi Jewish Sub 3324 A=0.7554 C=0.2446
gnomAD - Genomes East Asian Sub 3126 A=0.3260 C=0.6740
gnomAD - Genomes Other Sub 2154 A=0.6226 C=0.3774
14KJPN JAPANESE Study-wide 28256 A=0.26550 C=0.73450
8.3KJPN JAPANESE Study-wide 16758 A=0.26936 C=0.73064
1000Genomes_30x Global Study-wide 6404 A=0.5871 C=0.4129
1000Genomes_30x African Sub 1786 A=0.7307 C=0.2693
1000Genomes_30x Europe Sub 1266 A=0.6580 C=0.3420
1000Genomes_30x South Asian Sub 1202 A=0.6739 C=0.3261
1000Genomes_30x East Asian Sub 1170 A=0.3214 C=0.6786
1000Genomes_30x American Sub 980 A=0.445 C=0.555
1000Genomes Global Study-wide 5008 A=0.5829 C=0.4171
1000Genomes African Sub 1322 A=0.7315 C=0.2685
1000Genomes East Asian Sub 1008 A=0.3185 C=0.6815
1000Genomes Europe Sub 1006 A=0.6531 C=0.3469
1000Genomes South Asian Sub 978 A=0.672 C=0.328
1000Genomes American Sub 694 A=0.457 C=0.543
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.5969 C=0.4031
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.6484 C=0.3516
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.6535 C=0.3465
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.3259 C=0.6741, T=0.0000
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 A=0.5288 C=0.4712
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 A=0.351 C=0.649
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.657 C=0.343
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.740 C=0.260
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.666 C=0.334
HGDP-CEPH-db Supplement 1 Africa Sub 242 A=0.550 C=0.450
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.074 C=0.926
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.61 C=0.39
HapMap Global Study-wide 1890 A=0.5857 C=0.4143
HapMap American Sub 768 A=0.549 C=0.451
HapMap African Sub 692 A=0.721 C=0.279
HapMap Asian Sub 254 A=0.256 C=0.744
HapMap Europe Sub 176 A=0.688 C=0.312
Korean Genome Project KOREAN Study-wide 1832 A=0.3412 C=0.6588
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.666 C=0.334
CNV burdens in cranial meningiomas Global Study-wide 790 A=0.380 C=0.620
CNV burdens in cranial meningiomas CRM Sub 790 A=0.380 C=0.620
Northern Sweden ACPOP Study-wide 600 A=0.587 C=0.413
SGDP_PRJ Global Study-wide 390 A=0.318 C=0.682
Qatari Global Study-wide 216 A=0.694 C=0.306
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 68 A=0.68 C=0.32
The Danish reference pan genome Danish Study-wide 40 A=0.57 C=0.42
Siberian Global Study-wide 38 A=0.24 C=0.76
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 11 NC_000011.10:g.73241355A>C
GRCh38.p14 chr 11 NC_000011.10:g.73241355A>T
GRCh37.p13 chr 11 NC_000011.9:g.72952400A>C
GRCh37.p13 chr 11 NC_000011.9:g.72952400A>T
Gene: P2RY2, purinergic receptor P2Y2 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
P2RY2 transcript variant 2 NM_002564.4:c.*6062= N/A 3 Prime UTR Variant
P2RY2 transcript variant 3 NM_176071.3:c.*6062= N/A 3 Prime UTR Variant
P2RY2 transcript variant 1 NM_176072.3:c.*6062= N/A 3 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 A= C T
GRCh38.p14 chr 11 NC_000011.10:g.73241355= NC_000011.10:g.73241355A>C NC_000011.10:g.73241355A>T
GRCh37.p13 chr 11 NC_000011.9:g.72952400= NC_000011.9:g.72952400A>C NC_000011.9:g.72952400A>T
P2RY2 transcript variant 2 NM_002564.4:c.*6062= NM_002564.4:c.*6062A>C NM_002564.4:c.*6062A>T
P2RY2 transcript variant 2 NM_002564.3:c.*6062= NM_002564.3:c.*6062A>C NM_002564.3:c.*6062A>T
P2RY2 transcript variant 1 NM_176072.3:c.*6062= NM_176072.3:c.*6062A>C NM_176072.3:c.*6062A>T
P2RY2 transcript variant 1 NM_176072.2:c.*6062= NM_176072.2:c.*6062A>C NM_176072.2:c.*6062A>T
P2RY2 transcript variant 3 NM_176071.3:c.*6062= NM_176071.3:c.*6062A>C NM_176071.3:c.*6062A>T
P2RY2 transcript variant 3 NM_176071.2:c.*6062= NM_176071.2:c.*6062A>C NM_176071.2:c.*6062A>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#.

119 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss5848865 Feb 20, 2003 (111)
2 BCM_SSAHASNP ss10690823 Jul 11, 2003 (116)
3 WI_SSAHASNP ss12160700 Jul 11, 2003 (116)
4 CSHL-HAPMAP ss16518088 Feb 27, 2004 (120)
5 CSHL-HAPMAP ss19195628 Feb 27, 2004 (120)
6 CSHL-HAPMAP ss19905691 Feb 27, 2004 (120)
7 SSAHASNP ss20813875 Apr 05, 2004 (121)
8 ABI ss38700757 Mar 13, 2006 (126)
9 ILLUMINA ss67331648 Nov 30, 2006 (127)
10 ILLUMINA ss67731166 Nov 30, 2006 (127)
11 ILLUMINA ss68228442 Dec 12, 2006 (127)
12 PERLEGEN ss69320415 May 17, 2007 (127)
13 ILLUMINA ss70802318 May 25, 2008 (130)
14 ILLUMINA ss71381323 May 17, 2007 (127)
15 ILLUMINA ss75637812 Dec 06, 2007 (129)
16 HGSV ss78123424 Dec 06, 2007 (129)
17 KRIBB_YJKIM ss84260716 Dec 15, 2007 (130)
18 BGI ss102976017 Dec 01, 2009 (131)
19 1000GENOMES ss110652976 Jan 25, 2009 (130)
20 1000GENOMES ss114781237 Jan 25, 2009 (130)
21 ILLUMINA ss154292554 Dec 01, 2009 (131)
22 GMI ss156473174 Dec 01, 2009 (131)
23 ILLUMINA ss159469500 Dec 01, 2009 (131)
24 ILLUMINA ss160676217 Dec 01, 2009 (131)
25 ENSEMBL ss161448782 Dec 01, 2009 (131)
26 COMPLETE_GENOMICS ss170229287 Jul 04, 2010 (132)
27 ILLUMINA ss173724523 Jul 04, 2010 (132)
28 COMPLETE_GENOMICS ss175183768 Jul 04, 2010 (132)
29 BUSHMAN ss202872852 Jul 04, 2010 (132)
30 1000GENOMES ss225310581 Jul 14, 2010 (132)
31 1000GENOMES ss235609622 Jul 15, 2010 (132)
32 1000GENOMES ss242232111 Jul 15, 2010 (132)
33 GMI ss281064148 May 04, 2012 (137)
34 PJP ss291071928 May 09, 2011 (134)
35 ILLUMINA ss480935558 May 04, 2012 (137)
36 ILLUMINA ss480955072 May 04, 2012 (137)
37 ILLUMINA ss481919388 Sep 08, 2015 (146)
38 ILLUMINA ss485262763 May 04, 2012 (137)
39 ILLUMINA ss537232025 Sep 08, 2015 (146)
40 TISHKOFF ss562647023 Apr 25, 2013 (138)
41 SSMP ss658163199 Apr 25, 2013 (138)
42 ILLUMINA ss778535054 Sep 08, 2015 (146)
43 ILLUMINA ss783077311 Sep 08, 2015 (146)
44 ILLUMINA ss784035004 Sep 08, 2015 (146)
45 ILLUMINA ss832335560 Sep 08, 2015 (146)
46 ILLUMINA ss832980978 Jul 13, 2019 (153)
47 ILLUMINA ss833991621 Sep 08, 2015 (146)
48 EVA-GONL ss988669345 Aug 21, 2014 (142)
49 JMKIDD_LAB ss1077829088 Aug 21, 2014 (142)
50 1000GENOMES ss1341861077 Aug 21, 2014 (142)
51 DDI ss1426674232 Apr 01, 2015 (144)
52 EVA_GENOME_DK ss1575791287 Apr 01, 2015 (144)
53 EVA_DECODE ss1598330543 Apr 01, 2015 (144)
54 EVA_UK10K_ALSPAC ss1626882642 Apr 01, 2015 (144)
55 EVA_UK10K_TWINSUK ss1669876675 Apr 01, 2015 (144)
56 EVA_SVP ss1713263791 Apr 01, 2015 (144)
57 ILLUMINA ss1752031290 Sep 08, 2015 (146)
58 HAMMER_LAB ss1806874094 Sep 08, 2015 (146)
59 WEILL_CORNELL_DGM ss1932027344 Feb 12, 2016 (147)
60 GENOMED ss1967390567 Jul 19, 2016 (147)
61 JJLAB ss2026757595 Sep 14, 2016 (149)
62 USC_VALOUEV ss2155068054 Dec 20, 2016 (150)
63 HUMAN_LONGEVITY ss2183490556 Dec 20, 2016 (150)
64 SYSTEMSBIOZJU ss2627853110 Nov 08, 2017 (151)
65 ILLUMINA ss2632850207 Nov 08, 2017 (151)
66 GRF ss2699363425 Nov 08, 2017 (151)
67 GNOMAD ss2901339105 Nov 08, 2017 (151)
68 SWEGEN ss3008336492 Nov 08, 2017 (151)
69 BIOINF_KMB_FNS_UNIBA ss3027176173 Nov 08, 2017 (151)
70 CSHL ss3349665095 Nov 08, 2017 (151)
71 ILLUMINA ss3626688915 Oct 12, 2018 (152)
72 ILLUMINA ss3630866274 Oct 12, 2018 (152)
73 ILLUMINA ss3632989938 Oct 12, 2018 (152)
74 ILLUMINA ss3633689505 Oct 12, 2018 (152)
75 ILLUMINA ss3634462833 Oct 12, 2018 (152)
76 ILLUMINA ss3635381022 Oct 12, 2018 (152)
77 ILLUMINA ss3636146060 Oct 12, 2018 (152)
78 ILLUMINA ss3637131893 Oct 12, 2018 (152)
79 ILLUMINA ss3637915197 Oct 12, 2018 (152)
80 ILLUMINA ss3638971233 Oct 12, 2018 (152)
81 ILLUMINA ss3639796705 Oct 12, 2018 (152)
82 ILLUMINA ss3640170172 Oct 12, 2018 (152)
83 ILLUMINA ss3642912893 Oct 12, 2018 (152)
84 ILLUMINA ss3643848785 Oct 12, 2018 (152)
85 EGCUT_WGS ss3675655583 Jul 13, 2019 (153)
86 EVA_DECODE ss3692070573 Jul 13, 2019 (153)
87 ACPOP ss3738300123 Jul 13, 2019 (153)
88 ILLUMINA ss3744763654 Jul 13, 2019 (153)
89 EVA ss3749474785 Jul 13, 2019 (153)
90 ILLUMINA ss3772263511 Jul 13, 2019 (153)
91 PACBIO ss3786991073 Jul 13, 2019 (153)
92 PACBIO ss3792126250 Jul 13, 2019 (153)
93 PACBIO ss3797008601 Jul 13, 2019 (153)
94 KHV_HUMAN_GENOMES ss3814810905 Jul 13, 2019 (153)
95 EVA ss3832697719 Apr 26, 2020 (154)
96 EVA ss3839907815 Apr 26, 2020 (154)
97 EVA ss3845387957 Apr 26, 2020 (154)
98 HGDP ss3847422059 Apr 26, 2020 (154)
99 SGDP_PRJ ss3876561909 Apr 26, 2020 (154)
100 KRGDB ss3924965350 Apr 26, 2020 (154)
101 KOGIC ss3970223039 Apr 26, 2020 (154)
102 EVA ss3984652912 Apr 26, 2021 (155)
103 EVA ss3985540721 Apr 26, 2021 (155)
104 EVA ss4017544768 Apr 26, 2021 (155)
105 TOPMED ss4890331214 Apr 26, 2021 (155)
106 TOMMO_GENOMICS ss5202662336 Apr 26, 2021 (155)
107 1000G_HIGH_COVERAGE ss5287940861 Oct 16, 2022 (156)
108 EVA ss5315555125 Oct 16, 2022 (156)
109 EVA ss5400502766 Oct 16, 2022 (156)
110 HUGCELL_USP ss5483046586 Oct 16, 2022 (156)
111 1000G_HIGH_COVERAGE ss5583918599 Oct 16, 2022 (156)
112 SANFORD_IMAGENETICS ss5651512432 Oct 16, 2022 (156)
113 TOMMO_GENOMICS ss5750761383 Oct 16, 2022 (156)
114 EVA ss5799846310 Oct 16, 2022 (156)
115 YY_MCH ss5812542703 Oct 16, 2022 (156)
116 EVA ss5836857860 Oct 16, 2022 (156)
117 EVA ss5850034451 Oct 16, 2022 (156)
118 EVA ss5920555463 Oct 16, 2022 (156)
119 EVA ss5942823693 Oct 16, 2022 (156)
120 1000Genomes NC_000011.9 - 72952400 Oct 12, 2018 (152)
121 1000Genomes_30x NC_000011.10 - 73241355 Oct 16, 2022 (156)
122 The Avon Longitudinal Study of Parents and Children NC_000011.9 - 72952400 Oct 12, 2018 (152)
123 Genetic variation in the Estonian population NC_000011.9 - 72952400 Oct 12, 2018 (152)
124 The Danish reference pan genome NC_000011.9 - 72952400 Apr 26, 2020 (154)
125 gnomAD - Genomes NC_000011.10 - 73241355 Apr 26, 2021 (155)
126 Genome of the Netherlands Release 5 NC_000011.9 - 72952400 Apr 26, 2020 (154)
127 HGDP-CEPH-db Supplement 1 NC_000011.8 - 72630048 Apr 26, 2020 (154)
128 HapMap NC_000011.10 - 73241355 Apr 26, 2020 (154)
129 KOREAN population from KRGDB NC_000011.9 - 72952400 Apr 26, 2020 (154)
130 Korean Genome Project NC_000011.10 - 73241355 Apr 26, 2020 (154)
131 Northern Sweden NC_000011.9 - 72952400 Jul 13, 2019 (153)
132 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000011.9 - 72952400 Apr 26, 2021 (155)
133 CNV burdens in cranial meningiomas NC_000011.9 - 72952400 Apr 26, 2021 (155)
134 Qatari NC_000011.9 - 72952400 Apr 26, 2020 (154)
135 SGDP_PRJ NC_000011.9 - 72952400 Apr 26, 2020 (154)
136 Siberian NC_000011.9 - 72952400 Apr 26, 2020 (154)
137 8.3KJPN NC_000011.9 - 72952400 Apr 26, 2021 (155)
138 14KJPN NC_000011.10 - 73241355 Oct 16, 2022 (156)
139 TopMed NC_000011.10 - 73241355 Apr 26, 2021 (155)
140 UK 10K study - Twins NC_000011.9 - 72952400 Oct 12, 2018 (152)
141 ALFA NC_000011.10 - 73241355 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)
rs59561860 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
99951, ss78123424, ss110652976, ss114781237, ss170229287, ss175183768, ss202872852, ss281064148, ss291071928, ss480935558, ss1598330543, ss1713263791, ss3638971233, ss3639796705, ss3642912893, ss3643848785, ss3847422059 NC_000011.8:72630047:A:C NC_000011.10:73241354:A:C (self)
54402973, 30196115, 21393831, 2621122, 13473442, 32142744, 11584988, 766648, 202390, 14069274, 28578889, 7584408, 60631643, 30196115, ss225310581, ss235609622, ss242232111, ss480955072, ss481919388, ss485262763, ss537232025, ss562647023, ss658163199, ss778535054, ss783077311, ss784035004, ss832335560, ss832980978, ss833991621, ss988669345, ss1077829088, ss1341861077, ss1426674232, ss1575791287, ss1626882642, ss1669876675, ss1752031290, ss1806874094, ss1932027344, ss1967390567, ss2026757595, ss2155068054, ss2627853110, ss2632850207, ss2699363425, ss2901339105, ss3008336492, ss3349665095, ss3626688915, ss3630866274, ss3632989938, ss3633689505, ss3634462833, ss3635381022, ss3636146060, ss3637131893, ss3637915197, ss3640170172, ss3675655583, ss3738300123, ss3744763654, ss3749474785, ss3772263511, ss3786991073, ss3792126250, ss3797008601, ss3832697719, ss3839907815, ss3876561909, ss3924965350, ss3984652912, ss3985540721, ss4017544768, ss5202662336, ss5315555125, ss5400502766, ss5651512432, ss5799846310, ss5836857860, ss5942823693 NC_000011.9:72952399:A:C NC_000011.10:73241354:A:C (self)
71444534, 384004030, 636089, 26601040, 84598487, 105876870, 328857663, ss2183490556, ss3027176173, ss3692070573, ss3814810905, ss3845387957, ss3970223039, ss4890331214, ss5287940861, ss5483046586, ss5583918599, ss5750761383, ss5812542703, ss5850034451, ss5920555463 NC_000011.10:73241354:A:C NC_000011.10:73241354:A:C (self)
ss10690823, ss12160700 NT_033927.5:3151428:A:C NC_000011.10:73241354:A:C (self)
ss16518088, ss19195628, ss19905691, ss20813875 NT_033927.6:3151428:A:C NC_000011.10:73241354:A:C (self)
ss5848865, ss38700757, ss67331648, ss67731166, ss68228442, ss69320415, ss70802318, ss71381323, ss75637812, ss84260716, ss102976017, ss154292554, ss156473174, ss159469500, ss160676217, ss161448782, ss173724523 NT_167190.1:18258194:A:C NC_000011.10:73241354:A:C (self)
32142744, ss3924965350 NC_000011.9:72952399:A:T NC_000011.10:73241354:A:T (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

3 citations for rs4382936
PMID Title Author Year Journal
19710694 The purinergic receptor P2Y, G-protein coupled, 2 (P2RY2) gene associated with essential hypertension in Japanese men. Wang Z et al. 2010 Journal of human hypertension
19763137 Purinergic receptor P2Y, G-protein coupled, 2 (P2RY2) gene is associated with cerebral infarction in Japanese subjects. Wang Z et al. 2009 Hypertension research
19797825 Association of the purinergic receptor P2Y, G-protein coupled, 2 (P2RY2) gene with myocardial infarction in Japanese men. Wang ZX et al. 2009 Circulation journal
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