rs118203921(C;C)

common in clinvar

Is a	genotype
of	rs118203921
Gene	PAH
Chromosome	12
Position	102,852,881
Merged from	Rs28934900
mentioned	by

Magnitude

0

Repute

Good

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