{{Rsnum
|rsid=267606791
|Chromosome=X
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=F8
|position=154902150
|Gene_s=F8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNACC=RCV000011016.1
|CLNALLE=1
|CLNDBN=Hereditary factor VIII deficiency disease
|CLNDSDB=GeneReviews:MedGen:OMIM:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1404:C0019069:134500:306700:98878:28293008
|CLNHGVS=NC_000023.10:g.154130425C>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300841.0220
|Disease=Hereditary factor VIII deficiency disease
|FwdALT=T
|FwdREF=G
|GENEINFO=F8:2157
|GENE_ID=2157
|GENE_NAME=F8
|REF=C
|RSPOS=154130425
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606791
}}