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rs794726662

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794726662(-;GGC)
Make rs794726662(GGC;GGC)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position67942701
GeneLCAT
is asnp
is mentioned by
dbSNPrs794726662
ClinGenrs794726662
ebirs794726662
HLIrs794726662
Exacrs794726662
Varsomers794726662
Maprs794726662
PheGenIrs794726662
hapmaprs794726662
1000 genomesrs794726662
hgdprs794726662
ensemblrs794726662
gopubmedrs794726662
geneviewrs794726662
scholarrs794726662
googlers794726662
pharmgkbrs794726662
gwascentralrs794726662
openSNPrs794726662
23andMers794726662
23andMe allrs794726662
SNP Nexus

SNPshotrs794726662
SNPdbers794726662
MSV3drs794726662
GWAS Ctlgrs794726662
Max Magnitude0
ClinVar
Risk rs794726662(GCG;GCG)
Alt rs794726662(GCG;GCG)
Reference Rs794726662(;)
Significance Pathogenic
Disease Norum disease
Variation info
Gene LCAT
CLNDBN Norum disease
Reversed 1
HGVS NC_000016.9:g.67976604_67976605insGCC
CLNSRC OMIM Allelic Variant
CLNACC RCV000003843.3,