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rs797044919

From SNPedia

ClinVar
Risk rs797044919(C;C)
Alt rs797044919(C;C)
Reference rs797044919(;)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene CHD7
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000008.10:g.61757924dupC
CLNSRC
CLNACC RCV000190754.1,