{{Rsnum
|rsid = 28940888
|Gene = LCAT
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=16
|position=67940193
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LCAT
}}{{omim
|desc=LCAT DEFICIENCY
|id=606967
|rsnum=28940888
|variant=0015
}}

{{ClinVar
|rsid=28940888
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=67974096
|CHROM=16
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=LCAT:3931
|GENE_NAME=LCAT
|GENE_ID=3931
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.67974096G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606967.0015
|CLNSIG=5
|CLNCUI=C0023195
|CLNDBN=Norum disease
|Disease=Norum disease
|CLNACC=RCV000003855.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C0023195:245900:650:79293
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}