{{Rsnum
|rsid=13306487
|Gene=ITGB3
|Chromosome=17
|position=47292422
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.006887
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ITGB3
}}{{omim
|desc=Ca/Tu ALLOANTIGEN POLYMORPHISM
|id=173470
|rsnum=13306487
|variant=0009
}}{{ClinVar
|rsid=13306487
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=45369788
|CHROM=17
|GMAF=0.0069
|dbSNPBuildID=121
|SSR=0
|SAO=1
|VP=0x050260000000010516110100
|GENEINFO=ITGB3:3690
|GENE_NAME=ITGB3
|GENE_ID=3690
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.45369788G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9931; 0.006887
|CLNACC=RCV000014528.1; RCV000014529.18
|CLNDBN=Ca/Tu ALLOANTIGEN POLYMORPHISM; Thrombocytopenia, neonatal alloimmune
|CLNDSDB=MedGen
|CLNDSDBID=C0473780
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=173470.0009
|COMMON=1
|Disease=Ca/Tu ALLOANTIGEN POLYMORPHISM; Thrombocytopenia
}}