{{Rsnum
|rsid=137852224
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=F9
|position=139537111
|Gene_s=F9
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300746
|variant=0012
|rsnum=137852224
}}{{ClinVar
|rsid=137852224
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=138619270
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=F9:2158
|GENE_NAME=F9
|GENE_ID=2158
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.138619270T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300746.0012
|CLNSIG=5
|CLNCUI=C0008533
|CLNDBN=Hereditary factor IX deficiency disease
|Disease=Hereditary factor IX deficiency disease
|CLNACC=RCV000011314.6
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1495:C0008533:306900:98879:41788008
}}