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rs118203921(C;C)

From SNPedia

common in clinvar
Is agenotype
ofrs118203921
GenePAH
Chromosome12
Position102,852,881
Merged fromRs28934900
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Carrier of a phenylketonuria mutation