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rs202183605(C;C)

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common in clinvar

Is a	genotype
of	rs202183605
Gene	PAH
Chromosome	12
Position	102,844,432
mentioned	by

0

Good

Geno	Mag	Summary
(A;C)	3	Carrier of a phenylketonuria mutation
(C;C)	0	common in clinvar
(C;T)	3	Carrier of a phenylketonuria mutation

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Is a genotype