{{Rsnum
|rsid=119465999
|Gene=CIRH1A
|Chromosome=16
|position=69199289
|Orientation=minus
|GMAF=0.002296
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{omim
|id=607456
|rsnum=119465999
|variant=0001
}}{{ClinVar
|ALT=T
|CAF=0.9977; 0.002296
|CHROM=16
|CLNACC=RCV000003345.4
|CLNALLE=1
|CLNDBN=North american indian childhood cirrhosis
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1858051:604901:168583
|CLNHGVS=NC_000016.9:g.69199289C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=GTR; OMIM Allelic Variant
|CLNSRCID=GTR000205309; 607456.0001
|COMMON=1
|Disease=North american indian childhood cirrhosis
|FwdALT=T
|FwdREF=C
|GENEINFO=CIRH1A:84916
|GENE_ID=84916
|GENE_NAME=CIRH1A
|REF=C
|RSPOS=69199289
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000016110100
|WGT=0
|dbSNPBuildID=132
|rsid=119465999
}}