{{Rsnum
|rsid=28933678
|Gene=F8
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=T
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=X
|position=154904518
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=F8
}}{{omim
|desc=[[Hemophilia]] A
|id=306700
|rsnum=28933678
|variant=0203
}}
{{ neighbor
| rsid = 28933679
| distance = 7
}}

{{ neighbor
| rsid = 28933677
| distance = 321
}}
{{omim
|id=306700
|rsnum=28933678
|variant=0204
}}{{ClinVar
|rsid=28933678
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=154132793
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=F8:2157
|GENE_NAME=F8
|GENE_ID=2157
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000023.10:g.154132793C>T
|CLNORIGIN=1
|CLNSRCID=
300841.0203
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000010999.3
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDBN=Hereditary factor VIII deficiency disease
|CLNDSDB=GeneReviews:MedGen:OMIM:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1404:C0019069:134500:306700:98878:28293008
|CLNSRC=OMIM Allelic Variant
|Disease=Hereditary factor VIII deficiency disease
}}