{{Rsnum
|rsid=121918260
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PNPLA2
|position=823801
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|Gene_s=PNPLA2,RN5S2
}}{{omim
|id=609059
|rsnum=121918260
|variant=0004
}}{{ClinVar
|rsid=121918260
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=823801
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=PNPLA2:57104
|GENE_NAME=PNPLA2
|GENE_ID=57104
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.823801C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609059.0004
|CLNSIG=5
|CLNCUI=C1853136
|CLNDBN=Neutral lipid storage disease with myopathy
|Disease=Neutral lipid storage disease with myopathy
|CLNACC=RCV000001953.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1853136:610717:98908
}}