rs121917885

Orientation

minus

Stabilized

minus

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

Make rs121917885(A;A)

Make rs121917885(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

151338079

Gene	MED12L, P2RY12

is a	snp
is	mentioned by
dbSNP	rs121917885
dbSNP (classic)	rs121917885
ClinGen	rs121917885
ebi	rs121917885
HLI	rs121917885
Exac	rs121917885
Gnomad	rs121917885
Varsome	rs121917885
LitVar	rs121917885
Map	rs121917885
PheGenI	rs121917885
Biobank	rs121917885
1000 genomes	rs121917885
hgdp	rs121917885
ensembl	rs121917885
geneview	rs121917885
scholar	rs121917885
google	rs121917885
pharmgkb	rs121917885
gwascentral	rs121917885
openSNP	rs121917885
23andMe	rs121917885
SNPshot	rs121917885
SNPdbe	rs121917885
MSV3d	rs121917885
GWAS Ctlg	rs121917885

Max Magnitude

0

ClinVar
Risk	rs121917885(A;A)
Alt	rs121917885(A;A)
Reference	Rs121917885(G;G)
Significance	Pathogenic
Disease	Platelet-type bleeding disorder 8
Variation	info
Gene	P2RY12 MED12L
CLNDBN	Platelet-type bleeding disorder 8
Reversed	1
HGVS	NC_000003.11:g.151055867C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000009650.5,