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rs5030858(C;C)

From SNPedia

common in clinvar
Is agenotype
ofrs5030858
GenePAH
Chromosome12
Position102,840,493
Merged fromRs28934898
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Carrier of a phenylketonuria mutation
(T;T) 6 Phenylketonuria