{{Rsnum
|rsid=137852369
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=F8
|position=154904083
|Gene_s=F8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=306700
|variant=0057
|rsnum=137852369
}}{{ClinVar
|rsid=137852369
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=154132358
|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.154132358T>C
|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=RCV000010853.5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300841.0057
}}