{{Rsnum
|rsid=387906434
|Chromosome=X
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GTTT)
|geno3=(GTTT;GTTT)
|Gene=F8
|position=154999534
|Gene_s=F8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=X
|CLNACC=RCV000010872.1
|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.154227809_154227812delAAAC
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300841.0076
|Disease=Hereditary factor VIII deficiency disease
|FwdREF=TTTG
|REF=CAAAC
|RSPOS=154227808
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD
|VC=DIV
|VP=0x050060000000000002100200
|WGT=0
|dbSNPBuildID=137
|rsid=387906434
|GENEINFO=F8:2157
|GENE_ID=2157
|GENE_NAME=F8
}}