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rs797044894

From SNPedia

ClinVar
Risk rs797044894(G;G)
Alt rs797044894(G;G)
Reference rs797044894(;)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene KAT6B
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000010.10:g.76788683dupG
CLNSRC
CLNACC RCV000190717.1,