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rs28940886

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in clinvar
Make rs28940886(A;A)
Make rs28940886(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position67942939
GeneLCAT
is asnp
is mentioned by
dbSNPrs28940886
ebirs28940886
HLIrs28940886
Exacrs28940886
Varsomers28940886
Maprs28940886
PheGenIrs28940886
hapmaprs28940886
1000 genomesrs28940886
hgdprs28940886
ensemblrs28940886
gopubmedrs28940886
geneviewrs28940886
scholarrs28940886
googlers28940886
pharmgkbrs28940886
gwascentralrs28940886
openSNPrs28940886
23andMers28940886
23andMe allrs28940886
SNP Nexus

SNPshotrs28940886
SNPdbers28940886
MSV3drs28940886
GWAS Ctlgrs28940886
Max Magnitude0
OMIM606967
DescLCAT DEFICIENCY
Variant0012
Relatedalso
Neighborrs28940887
Distance220


ClinVar
Risk rs28940886(A;A)
Alt rs28940886(A;A)
Reference rs28940886(G;G)
Significance Pathogenic
Disease Norum disease
Variation info
Gene LCAT
CLNDBN Norum disease
Reversed 1
HGVS NC_000016.9:g.67976842C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003852.3,