{{Rsnum
|rsid=387906444
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=F8
|position=154965995
|Gene_s=F8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=X
|CLNACC=RCV000010928.1
|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.154194270T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300841.0132
|Disease=Hereditary factor VIII deficiency disease
|FwdALT=G
|FwdREF=A
|REF=T
|RSPOS=154194270
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=387906444
|GENEINFO=F8:2157
|GENE_ID=2157
|GENE_NAME=F8
}}