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rs797044636

From SNPedia

ClinVar
Risk rs797044636(C;C)
Alt rs797044636(C;C)
Reference rs797044636(;)
Significance Pathogenic
Disease Meckel syndrome type 6
Variation info
Gene CC2D2A
CLNDBN Meckel syndrome type 6
Reversed 0
HGVS NC_000004.11:g.15517627dupC
CLNSRC
CLNACC RCV000174035.1,