List of variants in gene PRDX3 reported as likely pathogenic for cerebellar disorder

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_006793.5(PRDX3):c.43C>T (p.Arg15Ter)	rs371560438	0.00004
NM_006793.5(PRDX3):c.508C>T (p.Arg170Ter)	rs140609531

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