{{Rsnum
|rsid=121908062
|Chromosome=17
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=GP1BA
|position=4933350
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GP1BA
}}{{omim
|id=606672
|rsnum=121908062
|variant=0003
}}{{ClinVar
|rsid=121908062
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=4836645
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GP1BA:2811
|GENE_NAME=GP1BA
|GENE_ID=2811
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.4836645G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606672.0003
|CLNSIG=5
|CLNCUI=C1280798
|CLNDBN=Pseudo von Willebrand disease
|Disease=Pseudo von Willebrand disease
|CLNACC=RCV000004370.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C1280798:177820:128115005
}}