rs200133991(C;C)

common in clinvar

Is a	genotype
of	rs200133991
Gene	C19orf12
Chromosome	19
Position	29,708,290
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	Carrier of a spastic paraplegia mutation