{{Rsnum
|rsid=34371500
|Chromosome=X
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=F8
|position=154969518
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=F8
}}{{omim
|id=306700
|rsnum=34371500
|variant=0103
}}

{{ClinVar
|rsid=34371500
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=154197793
|CHROM=X
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050268000601000502110100
|GENEINFO=F8:2157
|GENE_NAME=F8
|GENE_ID=2157
|WGT=1
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000023.10:g.154197793C>T
|CLNORIGIN=1
|CLNSIG=4
|CLNCUI=306700
|CLNDBN=Hereditary factor VIII deficiency disease
|Tags=RV;PM;PMC;S3D;NSN;REF;HD;GNO;OTHERKG;LSD;OM
|CLNDSDB=OMIM
|CLNDSDBID=306700
|Disease=Hereditary factor VIII deficiency disease
}}

{{PMID Auto
|PMID=18320046
|Title=Common variants within MECP2 confer risk of systemic lupus erythematosus.
|OA=1
}}

{{on chip | Illumina Human 1M}}