{{Rsnum
|rsid=121917885
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=P2RY12
|position=151338079
|Gene_s=MED12L,P2RY12
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=121917885
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=151055867
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=P2RY12:64805; MED12L:116931
|GENE_NAME=P2RY12; MED12L
|GENE_ID=64805; 116931
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.151055867C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600515.0002
|CLNSIG=5
|CLNCUI=C1853278
|CLNDBN=Platelet-type bleeding disorder 8
|Disease=Platelet-type bleeding disorder 8
|CLNACC=RCV000009650.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1853278:609821:36355
}}