List of variants in gene PDYN reported as uncertain significance for Autosomal dominant 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_024411.4(PDYN):c.-241G>C	rs574928545	0.00009
NM_024411.4(PDYN):c.-358G>A	rs745377265	0.00006
NM_024411.4(PDYN):c.-286G>C	rs886056538	0.00003
NM_024411.4(PDYN):c.-402C>G	rs775379753
NM_024411.5(PDYN):c.449_459delinsTAA	rs886056533
NM_024411.5(PDYN):c.700_703del	rs572674195

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