{{Rsnum
|rsid=28933681
|Gene=F8
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=X
|position=154904401
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=F8
}}{{omim
|desc=[[Hemophilia]] A
|id=306700
|rsnum=28933681
|variant=0209
}}
{{ neighbor
| rsid = 28933682
| distance = 319
}}

{{ neighbor
| rsid = 28933680
| distance = 92
}}

{{ClinVar
|rsid=28933681
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=154132676
|CHROM=X
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260000000000402110100
|GENEINFO=F8:2157
|GENE_NAME=F8
|GENE_ID=2157
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.154132676C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNCUI=306700
|CLNDBN=Hereditary factor VIII deficiency disease
|Tags=RV;PM;S3D;HD;OTHERKG;LSD;OM
|CLNACC=RCV000011005.3
|CLNDSDB=GeneReviews:MedGen:OMIM:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1404:C0019069:134500:306700:98878:28293008
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300841.0209
|Disease=Hereditary factor VIII deficiency disease
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}