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rs797044552

From SNPedia

ClinVar
Risk rs797044552(G;G)
Alt rs797044552(G;G)
Reference rs797044552(;)
Significance Pathogenic
Disease Mirror movements
Variation info
Gene DCC
CLNDBN Mirror movements, congenital
Reversed 0
HGVS NC_000018.9:g.50432572dupG
CLNSRC
CLNACC RCV000192078.1,