List of variants in gene combination PEX10, RER1 reported as likely benign for Zellweger spectrum disorders

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_002617.4(PEX10):c.*676C>T	rs77863194	0.00408
NM_002617.4(PEX10):c.*595G>A	rs72924937	0.00377

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