List of variants in gene combination LOC126861615, PAH reported by Inserm U 954, Faculté de Médecine de Nancy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000277.3(PAH):c.869A>T (p.His290Leu)	rs62642919
NM_000277.3(PAH):c.887A>G (p.Asp296Gly)	rs281865446
NM_000277.3(PAH):c.895T>C (p.Phe299Leu)	rs796064504
NM_000277.3(PAH):c.912+2T>C	rs281865449
NM_000277.3(PAH):c.912+3A>C	rs281865450

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