{{Rsnum
|rsid=36209567
|Gene=F7
|Chromosome=13
|position=113118668
|Orientation=plus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=F7
}}{{omim
|id=227500
|rsnum=36209567
|variant=0010
}}{{ClinVar
|rsid=36209567
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=113772982
|CHROM=13
|GMAF=0.0009
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050260000000000116110100
|GENEINFO=F7:2155
|GENE_NAME=F7
|GENE_ID=2155
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.113772982C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNCUI=227500
|CLNDBN=Factor VII deficiency
|Tags=PM;S3D;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNACC=RCV000012857.1
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0015503:227500:327:37193007
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613878.0010
|COMMON=0
|Disease=Factor VII deficiency
}}