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rs794726662

From SNPedia

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,