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rs62644499(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs62644499
GenePAH
Chromosome12
Position102,840,472
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 5.9 Non-phenylketonuria hyperphenylalaninemia genotype
(A;G) 3 Carrier of a non-phenylketonuria hyperphenylalaninemia allele
(G;G) 0 common in clinvar