{{Rsnum
|rsid=76811038
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ITGA2B
|position=44379780
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ITGA2B
}}{{omim
|id=607759
|rsnum=76811038
|variant=0013
}}
{{omim
|id=273800
|rsnum=76811038
}}{{ClinVar
|rsid=76811038
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=42457148
|CHROM=17
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=ITGA2B:3674
|GENE_NAME=ITGA2B
|GENE_ID=3674
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.42457148A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=607759.0013
|CLNSIG=5
|CLNCUI=C0040015
|CLNDBN=Glanzmann's thrombasthenia
|Disease=Glanzmann's thrombasthenia
|CLNACC=RCV000003034.1
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0040015:273800:849:32942005
}}{{PMID Auto
|PMID=9734640
|Title=Double heterozygosity of the GPIIb gene in a Swiss patient with Glanzmann's thrombasthenia.
}}

{{PMID Auto
|PMID=9920835
|Title=Molecular genetic analysis of a compound heterozygote for the glycoprotein (GP) IIb gene associated with Glanzmann's thrombasthenia: disruption of the 674-687 disulfide bridge in GPIIb prevents surface exposure of GPIIb-IIIa complexes.
}}