"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "PEX19"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 501546	NM_002857.4(PEX19):c.857C>T (p.Ser286Leu)	PEX19 (S286L)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance
Select item 293229	NM_002857.4(PEX19):c.433-11G>T	PEX19	Single nucleotide variant (intron variant)	Peroxisome biogenesis disorder 12A (Zellweger) +1 more	GBenign/Likely benign
Select item 293233	NM_002857.4(PEX19):c.181-15A>G	PEX19	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign

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