List of variants in gene PAH reported as uncertain significance by Genome-Nilou Lab

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000277.3(PAH):c.*19G>T	rs372637021	0.00126
NM_000277.3(PAH):c.158G>A (p.Arg53His)	rs118092776	0.00091
NM_000277.3(PAH):c.786C>T (p.Val262=)	rs776860902	0.00001
NM_000277.3(PAH):c.1089G>C (p.Lys363Asn)	rs63329263

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