rs786200861(TCT;TCT)

common in clinvar

Is a	genotype
of	rs786200861
Gene	PAH
Chromosome	12
Position	102,843,751
Merged into	Rs62516096
mentioned	by

Magnitude

0

Repute

Good

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