RS199475697 PAH

Health Risk Chr 12:102855229
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What This Variant Does
"CLNSIG=1
Associated Conditions
Phenylketonuria
Inborn genetic diseases
Phenylketonuria
Inborn genetic diseases
Other Variants in PAH
rs5030861 rs5030858 rs62642936 rs62514959 rs62508698 rs76296470 rs5030849 rs62516151 rs5030847 rs62514891
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