List of variants in gene PNPT1 reported as uncertain significance for cerebellar ataxia

Minimum submission review status:		Collection method:
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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_033109.5(PNPT1):c.1525G>A (p.Val509Ile)	rs146571352	0.00109
NM_033109.5(PNPT1):c.493C>T (p.Pro165Ser)	rs151166046	0.00006

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