{{Rsnum
|rsid=137852243
|Chromosome=X
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=F9
|position=139551223
|Gene_s=F9
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300746
|variant=0033
|rsnum=137852243
}}
{{omim
|id=300746
|variant=0034
|rsnum=137852243
}}{{ClinVar
|rsid=137852243
|Reversed=0
|FwdREF=G
|FwdALT=C,T
|REF=G
|ALT=C,T
|RSPOS=138633382
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=F9:2158
|GENE_NAME=F9
|GENE_ID=2158
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000023.10:g.138633382G>C; NC_000023.10:g.138633382G>T
|CLNORIGIN=1
|CLNSIG=5
|CLNCUI=
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000011340.1; RCV000011339.1
|CLNDBN=HEMOPHILIA B(M); Hereditary factor IX deficiency disease
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=CN043453; NBK1495:C0008533:306900:98879:41788008
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300746.0034; 300746.0033
|Disease=HEMOPHILIA B(M); Hereditary factor IX deficiency disease
}}