{{Rsnum
|rsid=121918448
|Gene=ITGB3
|Chromosome=17
|position=47292175
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=ITGB3
}}{{omim
|id=173470
|rsnum=121918448
|variant=0007
}}{{ClinVar
|rsid=121918448
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=45369541
|CHROM=17
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000016110100
|GENEINFO=ITGB3:3690
|GENE_NAME=ITGB3
|GENE_ID=3690
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.45369541C>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNACC=RCV000014525.1; RCV000014526.24
|CLNDBN=Mo ALLOANTIGEN POLYMORPHISM; Thrombocytopenia, neonatal alloimmune
|CLNDSDB=MedGen
|CLNDSDBID=C0473780
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=173470.0007
|COMMON=0
|Disease=Mo ALLOANTIGEN POLYMORPHISM; Thrombocytopenia
}}