List of variants in gene NOP56 reported as uncertain significance 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_006392.4(NOP56):c.452G>C (p.Ser151Thr)	rs1360494485	0.00001
NM_006392.4(NOP56):c.1475A>G (p.Gln492Arg)	rs2086850165

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