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rs796052664

From SNPedia

ClinVar
Risk rs796052664(CCT;CCT)
Alt rs796052664(CCT;CCT)
Reference rs796052664(TC;TC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62071002_62071003delGAinsAGG
CLNSRC
CLNACC RCV000187943.1,