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rs74486803(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs74486803
GenePAH
Chromosome12
Position102,855,315
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 5.9 Non-phenylketonuria hyperphenylalaninemia genotype
(A;C) 3 Carrier of a non-phenylketonuria hyperphenylalaninemia allele
(C;C) 0 common in clinvar
(C;T) 3 Carrier of a phenylketonuria mutation