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rs121917886

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917886(C;T)
Make rs121917886(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position151338053
GeneMED12L, P2RY12
is asnp
is mentioned by
dbSNPrs121917886
ebirs121917886
HLIrs121917886
Exacrs121917886
Varsomers121917886
Maprs121917886
PheGenIrs121917886
hapmaprs121917886
1000 genomesrs121917886
hgdprs121917886
ensemblrs121917886
gopubmedrs121917886
geneviewrs121917886
scholarrs121917886
googlers121917886
pharmgkbrs121917886
gwascentralrs121917886
openSNPrs121917886
23andMers121917886
23andMe allrs121917886
SNP Nexus

SNPshotrs121917886
SNPdbers121917886
MSV3drs121917886
GWAS Ctlgrs121917886
Max Magnitude0
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
CLNACC RCV000009651.3,