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rs797044889

From SNPedia

ClinVar
Risk rs797044889(;)
Alt rs797044889(;)
Reference rs797044889(CG;CG)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene IQSEC2
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000023.10:g.53279705_53279706delCG
CLNSRC
CLNACC RCV000190711.1,