{{Rsnum
|rsid=137852361
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=F8
|position=154928677
|Gene_s=F8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=306700
|variant=0028
|rsnum=137852361
}}{{ClinVar
|rsid=137852361
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=154156952
|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.154156952G>A
|CLNORIGIN=1
|CLNSIG=5
|CLNCUI=306700
|CLNDBN=Hereditary factor VIII deficiency disease
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1404:C0019069:134500:306700:98878:28293008
|Disease=Hereditary factor VIII deficiency disease
|CLNACC=RCV000010824.5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300841.0028
}}