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rs797044918

From SNPedia

ClinVar
Risk rs797044918(;)
Alt rs797044918(;)
Reference rs797044918(AAG;AAG)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene DYNC1H1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000014.8:g.102496267_102496269delAAG
CLNSRC
CLNACC RCV000190753.1,