rs118192224(C;C)

common in clinvar

Is a	genotype
of	rs118192224
Gene	KCNQ2
Chromosome	20
Position	63,419,632
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	Possible miscall; otherwise, benign familial neonatal seizure related mutation