{{Rsnum
|rsid=121965086
|Chromosome=10
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LIPA
|position=89225168
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LIPA
}}{{omim
|id=613497
|rsnum=121965086
|variant=0001
}}{{ClinVar
|rsid=121965086
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=90984925
|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.90984925A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=613497.0001
|CLNSIG=5
|CLNCUI=CN031408
|CLNDBN=Wolman disease; Lysosomal acid lipase deficiency
|Disease=Wolman disease; Lysosomal acid lipase deficiency
|CLNACC=RCV000000095.1; RCV000000096.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet:Orphanet
|CLNDSDBID=C0043208:278000:275761:75233:75234
}}