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rs797044859

From SNPedia

ClinVar
Risk rs797044859(;)
Alt rs797044859(;)
Reference rs797044859(AT;AT)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ARID1B
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000006.11:g.157521899_157521900delAT
CLNSRC
CLNACC RCV000190662.1,