rs121908523(A;G)

Carrier of a type I primary hyperoxaluria mutation

Is a	genotype
of	rs121908523
Gene	AGXT
Chromosome	2
Position	240,868,986
mentioned	by

Magnitude

3

Repute

Bad

Geno	Mag	Summary
(G;G)	0	common in clinvar

Unaffected in absence of a second AGXT gene mutation