"GenomeConnect - Invitae Patient Insights Network"[submitter] AND "PRX - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 476983	NM_181882.3(PRX):c.848T>G (p.Val283Gly)	PRX (V283G)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +1 more	GUncertain significance
Select item 216836	NM_181882.3(PRX):c.823C>A (p.Leu275Ile)	PRX (L275I)	Single nucleotide variant (3 prime UTR variant +1 more)	Charcot-Marie-Tooth disease type 4 +7 more	GConflicting classifications of pathogenicity