rs66521141(G;G)

common in clinvar

Is a	genotype
of	rs66521141
Gene	OTC
Chromosome	X
Position	38,367,367
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;A)	8.2	Ornithine Transcarbamylase Deficiency
(A;G)	3	Carrier of an ornithine carbamoyltransferase mutation
(G;G)	0	common in clinvar