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rs797044908

From SNPedia

ClinVar
Risk rs797044908(AA;AA)
Alt rs797044908(AA;AA)
Reference rs797044908(TG;TG)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene PHF6
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000023.10:g.133551279_133551280delTGinsAA
CLNSRC
CLNACC RCV000190736.1,