{{Rsnum
|rsid=104894854
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=GPC3
|position=133753628
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GPC3
}}{{omim
|id=300037
|rsnum=104894854
|variant=0003
}}{{ClinVar
|rsid=104894854
|Reversed=1
|FwdREF=T
|FwdALT=A
|REF=A
|ALT=T
|RSPOS=132887655
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GPC3:2719
|GENE_NAME=GPC3
|GENE_ID=2719
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.132887655A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300037.0003
|CLNSIG=5
|CLNCUI=C0796154
|CLNDBN=Simpson-Golabi-Behmel syndrome
|Disease=Simpson-Golabi-Behmel syndrome
|CLNACC=RCV000012453.21
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1219:C0796154:312870:373:439143004
}}