List of variants in gene PNKP reported as benign for cerebellar ataxia

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_007254.4(PNKP):c.498+23A>T	rs1290649	0.39505
NM_007254.4(PNKP):c.579G>A (p.Arg193=)	rs145904995	0.00205

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