{{Rsnum
|rsid=267607211
|Chromosome=16
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LCAT
|position=67942686
|Gene_s=LCAT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=16
|CLNACC=RCV000003841.1
|CLNALLE=1
|CLNDBN=Norum disease
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C0023195:245900:650:79293
|CLNHGVS=NC_000016.9:g.67976589A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606967.0001
|Disease=Norum disease
|FwdALT=C
|FwdREF=T
|GENEINFO=LCAT:3931
|GENE_ID=3931
|GENE_NAME=LCAT
|REF=A
|RSPOS=67976589
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607211
}}