{{Rsnum
|rsid = 28940886
|Gene = LCAT
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|Chromosome=16
|position=67942939
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LCAT
}}{{omim
|desc=LCAT DEFICIENCY
|id=606967
|rsnum=28940886
|variant=0012
}}
{{ neighbor
| rsid = 28940887
| distance = 220
}}

{{ClinVar
|rsid=28940886
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=67976842
|CHROM=16
|dbSNPBuildID=137
|SSR=0
|SAO=0
|VP=0x050060000000000002110100
|GENEINFO=LCAT:3931
|GENE_NAME=LCAT
|GENE_ID=3931
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.67976842C>T
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606967.0012
|CLNSIG=5
|CLNCUI=C0023195
|CLNDBN=Norum disease
|Disease=Norum disease
|CLNACC=RCV000003852.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C0023195:245900:650:79293
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}