rs6785930

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs6785930(A;A)

Make rs6785930(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

151338828

Gene	MED12L, P2RY12

is a	snp
is	mentioned by
dbSNP	rs6785930
dbSNP (classic)	rs6785930
ClinGen	rs6785930
ebi	rs6785930
HLI	rs6785930
Exac	rs6785930
Gnomad	rs6785930
Varsome	rs6785930
LitVar	rs6785930
Map	rs6785930
PheGenI	rs6785930
Biobank	rs6785930
1000 genomes	rs6785930
hgdp	rs6785930
ensembl	rs6785930
geneview	rs6785930
scholar	rs6785930
google	rs6785930
pharmgkb	rs6785930
gwascentral	rs6785930
openSNP	rs6785930
23andMe	rs6785930
SNPshot	rs6785930
SNPdbe	rs6785930
MSV3d	rs6785930
GWAS Ctlg	rs6785930

GMAF

0.264

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

[PMID 19786296] Platelet glycoprotein GP VI 13254C allele is an independent risk factor of premature myocardial infarction

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

ClinVar
Risk	rs6785930(A;A)
Alt	rs6785930(A;A)
Reference	Rs6785930(G;G)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	P2RY12 MED12L
CLNDBN	not specified
Reversed	0
HGVS	NC_000003.11:g.151056616G>A
CLNSRC
CLNACC	RCV000242918.1,