List of variants in gene PAH reported as benign by Quest Diagnostics Nichols Institute San Juan Capistrano

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.1278T>C (p.Asn426=)	rs59326968	0.04124
NM_000277.3(PAH):c.707-7A>T	rs62508624	0.02868
NM_000277.3(PAH):c.963C>T (p.Leu321=)	rs61747292	0.01582
NM_000277.3(PAH):c.1242C>T (p.Tyr414=)	rs1801152	0.00779

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