rs121917886

Orientation

minus

Stabilized

minus

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

Make rs121917886(C;T)

Make rs121917886(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

151338053

Gene	MED12L, P2RY12

is a	snp
is	mentioned by
dbSNP	rs121917886
dbSNP (classic)	rs121917886
ClinGen	rs121917886
ebi	rs121917886
HLI	rs121917886
Exac	rs121917886
Gnomad	rs121917886
Varsome	rs121917886
LitVar	rs121917886
Map	rs121917886
PheGenI	rs121917886
Biobank	rs121917886
1000 genomes	rs121917886
hgdp	rs121917886
ensembl	rs121917886
geneview	rs121917886
scholar	rs121917886
google	rs121917886
pharmgkb	rs121917886
gwascentral	rs121917886
openSNP	rs121917886
23andMe	rs121917886
SNPshot	rs121917886
SNPdbe	rs121917886
MSV3d	rs121917886
GWAS Ctlg	rs121917886

Max Magnitude

0

ClinVar
Risk	rs121917886(T;T)
Alt	rs121917886(T;T)
Reference	Rs121917886(C;C)
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.151055841G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000009651.5,