{{Rsnum
|rsid=121908054
|Chromosome=16
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=LCAT
|position=67940400
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LCAT
}}{{omim
|id=606967
|rsnum=121908054
|variant=0010
}}{{ClinVar
|rsid=121908054
|Reversed=1
|FwdREF=T
|FwdALT=A
|REF=A
|ALT=T
|RSPOS=67974303
|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.67974303A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606967.0010
|CLNSIG=5
|CLNCUI=C0023195
|CLNDBN=Norum disease
|Disease=Norum disease
|CLNACC=RCV000003850.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C0023195:245900:650:79293
}}