C4225237[trait identifier] AND "Mayo Clinic Laboratories, Mayo Clinic" - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 235376	NM_001351132.2(PEX5):c.815T>C (p.Met272Thr)	PEX5 (M272T +3 more)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign
Select item 559038	NM_001351132.2(PEX5):c.967-26C>G	PEX5	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 194614	NM_001351132.2(PEX5):c.1814G>A (p.Ser605Asn)	PEX5 (S597N +6 more)	Single nucleotide variant (missense variant)	Peroxisome biogenesis disorder 2A (Zellweger) +4 more	GUncertain significance

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