{{Rsnum
|rsid=121918299
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TJP2
|position=69216367
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TJP2
}}{{omim
|id=607709
|rsnum=121918299
|variant=0001
}}{{ClinVar
|rsid=121918299
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=71831283
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=TJP2:9414
|GENE_NAME=TJP2
|GENE_ID=9414
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.71831283T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607709.0001
|CLNSIG=5
|CLNCUI=C1843139
|CLNDBN=Hypercholanemia, familial
|Disease=Hypercholanemia
|CLNACC=RCV000003041.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1843139:607748:238475
}}