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rs796052388

From SNPedia

ClinVar
Risk rs796052388(;)
Alt rs796052388(;)
Reference rs796052388(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CNTNAP2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.146818167delA
CLNSRC
CLNACC RCV000187252.1,