{{Rsnum
|rsid=121965087
|Chromosome=10
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=LIPA
|position=89245776
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LIPA
}}{{omim
|id=613497
|rsnum=121965087
|variant=0006
}}{{ClinVar
|rsid=121965087
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=91005533
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=LIPA:3988
|GENE_NAME=LIPA
|GENE_ID=3988
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.91005533G>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000000102.1
|CLNDBN=Wolman disease
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613497.0006
|Disease=Wolman disease
}}