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rs797044903

From SNPedia

ClinVar
Risk rs797044903(;)
Alt rs797044903(;)
Reference rs797044903(GGGCCAA;GGGCCAA)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene PLA2G6
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000022.10:g.38528890_38528896delTTGGCCC
CLNSRC
CLNACC RCV000190729.1,