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rs118203925(C;T)

From SNPedia

Carrier of a non-phenylketonuria hyperphenylalaninemia allele
Is agenotype
ofrs118203925
GenePAH
Chromosome12
Position102,912,819
mentionedby
Magnitude3
ReputeBad
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

see hyperphenylalaninemia and the ClinVar link on the SNP page for this SNP