rs118203925(C;C)

common in clinvar

Is a	genotype
of	rs118203925
Gene	PAH
Chromosome	12
Position	102,912,819
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	Carrier of a non-phenylketonuria hyperphenylalaninemia allele
(T;T)	5.9	Non-phenylketonuria hyperphenylalaninemia genotype