List of variants reported as likely benign for Phenylketonuria by Inserm U 954, Faculté de Médecine de Nancy

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000277.3(PAH):c.169-42T>A	rs281865459	0.00001
NM_000277.3(PAH):c.612T>C (p.Tyr204=)	rs62514928	0.00001
NM_000277.3(PAH):c.1152C>G (p.Pro384=)	rs281865458
NM_000277.3(PAH):c.1199+70G>A	rs281865457

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