{{Rsnum
|rsid=5917
|Gene=ITGB3
|Chromosome=17
|position=47284587
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.003673
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ITGB3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.7 | 99.3
| JPT | 0.0 | 0.9 | 99.1
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.7 | 99.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 5.3 | 94.7
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=PEN(a)/PEN(b) ALLOANTIGEN POLYMORPHISM
|id=173470
|rsnum=5917
|variant=0005
}}

{{ClinVar
|rsid=5917
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=45361953
|CHROM=17
|GMAF=0.0037
|dbSNPBuildID=52
|SSR=0
|SAO=1
|VP=0x050260000000040517110101
|GENEINFO=ITGB3:3690
|GENE_NAME=ITGB3
|GENE_ID=3690
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.45361953G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9963; 0.003673
|CLNACC=RCV000014516.1; RCV000014517.24; RCV000014518.24
|CLNDBN=PEN(a)/PEN(b) ALLOANTIGEN POLYMORPHISM; Thrombocytopenia, neonatal alloimmune; Posttransfusion purpura
|CLNDSDB=MedGen
|CLNDSDBID=C0473780; C0398648
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=173470.0005
|COMMON=1
|Disease=PEN(a)/PEN(b) ALLOANTIGEN POLYMORPHISM; Thrombocytopenia; Posttransfusion purpura
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}