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rs863223386

From SNPedia

ClinVar
Risk
Alt
Reference Rs863223386(T;T)
Significance Pathogenic
Disease Abnormality of neuronal migration
Variation info
Gene VPS13B
CLNDBN Abnormality of neuronal migration
Reversed 0
HGVS NC_000008.10:g.100479778delT
CLNSRC
CLNACC RCV000201400.1,