{{Rsnum
|rsid=121918520
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=PRKCSH
|position=11448917
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRKCSH
}}{{omim
|id=177060
|rsnum=121918520
|variant=0005
}}{{ClinVar
|rsid=121918520
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=11559732
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=PRKCSH:5589
|GENE_NAME=PRKCSH
|GENE_ID=5589
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.11559732C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=177060.0005
|CLNSIG=5
|CLNCUI=C0158683
|CLNDBN=Congenital cystic disease of liver
|Disease=Congenital cystic disease of liver
|CLNACC=RCV000014147.24
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0158683:174050:2924:72925005
}}