List of variants in gene combination LOC126861615, PAH reported as likely benign for Phenylketonuria

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000277.3(PAH):c.894C>T (p.Ser298=)	rs765823928	0.00003
NM_000277.3(PAH):c.861G>A (p.Leu287=)	rs754686336	0.00002
NM_000277.3(PAH):c.870T>C (p.His290=)	rs751203209	0.00002
NM_000277.3(PAH):c.843-11C>G
NM_000277.3(PAH):c.843-9G>C	rs2136645008
NM_000277.3(PAH):c.858G>A (p.Glu286=)	rs556021587
NM_000277.3(PAH):c.861G>T (p.Leu287=)	rs754686336
NM_000277.3(PAH):c.867A>T (p.Gly289=)
NM_000277.3(PAH):c.876C>A (p.Pro292=)
NM_000277.3(PAH):c.888T>C (p.Asp296=)
NM_000277.3(PAH):c.912+15T>G
NM_000277.3(PAH):c.912+20G>T
NM_000277.3(PAH):c.912+9T>C

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