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rs121917885

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917885(A;A)
Make rs121917885(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position151338079
GeneMED12L, P2RY12
is asnp
is mentioned by
dbSNPrs121917885
ebirs121917885
HLIrs121917885
Exacrs121917885
Varsomers121917885
Maprs121917885
PheGenIrs121917885
hapmaprs121917885
1000 genomesrs121917885
hgdprs121917885
ensemblrs121917885
gopubmedrs121917885
geneviewrs121917885
scholarrs121917885
googlers121917885
pharmgkbrs121917885
gwascentralrs121917885
openSNPrs121917885
23andMers121917885
23andMe allrs121917885
SNP Nexus

SNPshotrs121917885
SNPdbers121917885
MSV3drs121917885
GWAS Ctlgrs121917885
Max Magnitude0
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
CLNACC RCV000009650.3,