{{Rsnum
|rsid=387906476
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=F9
|position=139530844
|Gene_s=F9
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=X
|CLNACC=RCV000011317.1
|CLNALLE=1
|CLNDBN=Hereditary factor IX deficiency disease
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1495:C0008533:306900:98879:41788008
|CLNHGVS=NC_000023.10:g.138613003A>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300746.0014
|Disease=Hereditary factor IX deficiency disease
|FwdALT=T
|FwdREF=A
|REF=A
|RSPOS=138613003
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;NSM;REF;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a01000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=387906476
}}