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rs794728981

From SNPedia

ClinVar
Risk rs794728981(;)
Alt rs794728981(;)
Reference rs794728981(GCTGAAAGTG;GCTGAAAGTG)
Significance Pathogenic
Disease not provided Inborn genetic diseases
Variation info
Gene BAG3
CLNDBN not provided Inborn genetic diseases
Reversed 0
HGVS NC_000010.10:g.121436333_121436342delCTGAAAGTGG
CLNSRC
CLNACC RCV000183323.1, RCV000190668.1,