{{Rsnum
|rsid=28933668
|Gene=F8
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=X
|position=154966522
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=F8
}}{{omim
|desc=[[Hemophilia]] A
|id=306700
|rsnum=28933668
|variant=0122
}}
{{ neighbor
| rsid = 28933670
| distance = 39
}}

{{ neighbor
| rsid = 28933669
| distance = 1
}}

{{omim
|id=306700
|rsnum=28933668
|variant=0121
}}

{{ClinVar
|rsid=28933668
|Reversed=1
|FwdREF=C
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=154194797
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=F8:2157
|GENE_NAME=F8
|GENE_ID=2157
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.154194797G>A
|CLNORIGIN=1
|CLNSRCID=
300841.0122
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000010918.1
|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
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}