rs6809699

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(C;C)	0	common on affy axiom data

Make rs6809699(A;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

151338810

Gene	MED12L, P2RY12

is a	snp
is	mentioned by
dbSNP	rs6809699
dbSNP (classic)	rs6809699
ClinGen	rs6809699
ebi	rs6809699
HLI	rs6809699
Exac	rs6809699
Gnomad	rs6809699
Varsome	rs6809699
LitVar	rs6809699
Map	rs6809699
PheGenI	rs6809699
Biobank	rs6809699
1000 genomes	rs6809699
hgdp	rs6809699
ensembl	rs6809699
geneview	rs6809699
scholar	rs6809699
google	rs6809699
pharmgkb	rs6809699
gwascentral	rs6809699
openSNP	rs6809699
23andMe	rs6809699
SNPshot	rs6809699
SNPdbe	rs6809699
MSV3d	rs6809699
GWAS Ctlg	rs6809699

GMAF

0.1097

Max Magnitude

0

?

(A;A) (A;C) (C;C)

28

[PMID 17707382] rs10935838, rs2046934, rs5853517, and rs6809699 venous thromboembolism lower risk of incident DVT/PE as compared to the reference haplotype H1 (odds ratio=0.50, 95% CI=0.27-0.93, p=0.028)

[PMID 25901734] Effect of platelet receptor gene polymorphisms on outcomes in ST-elevation myocardial infarction patients after percutaneous coronary intervention

[PMID 26083990] Influence of P2Y12 polymorphisms on platelet activity but not ex-vivo antiplatelet effect of ticagrelor in healthy Chinese male subjects

ClinVar
Risk	Rs6809699(C;C)
Alt	Rs6809699(C;C)
Reference	Rs6809699(A;A)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	P2RY12 MED12L
CLNDBN	not specified
Reversed	0
HGVS	NC_000003.11:g.151056598A>C
CLNSRC
CLNACC	RCV000245981.1,

[PMID 32256707 ] Association between P2RY12 Gene Polymorphisms and IVIG Resistance in Kawasaki Patients.