C3553947[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 262791	NM_002617.4(PEX10):c.913-4G>A	PEX10	Single nucleotide variant (intron variant)	not specified +4 more	GBenign
Select item 1180486	NM_002617.4(PEX10):c.776+33G>T	PEX10	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 964978	NM_002617.4(PEX10):c.725G>A (p.Arg242Gln)	PEX10 (R261Q +4 more)	Single nucleotide variant (missense variant +1 more)	Peroxisome biogenesis disorder, complementation group 7 +2 more	GUncertain significance
Select item 197385	NM_002617.4(PEX10):c.712G>C (p.Gly238Arg)	PEX10 (G258R +4 more)	Single nucleotide variant (missense variant +1 more)	Peroxisome biogenesis disorder 6A (Zellweger) +3 more	GConflicting classifications of pathogenicity
Select item 129884	NM_002617.4(PEX10):c.291A>G (p.Thr97=)	PEX10	Single nucleotide variant (synonymous variant +2 more)	not provided +4 more	GBenign
Select item 129883	NM_002617.4(PEX10):c.279C>T (p.Gly93=)	PEX10	Single nucleotide variant (synonymous variant +2 more)	not specified +4 more	GBenign
Select item 284321	NM_002617.4(PEX10):c.6C>G (p.Ala2=)	PEX10	Single nucleotide variant (synonymous variant +1 more)	Peroxisome biogenesis disorder, complementation group 7 +3 more	GBenign/Likely benign

ClinVar