List of variants in gene STUB1 reported as pathogenic for cerebellar degeneration

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_005861.4(STUB1):c.199G>A (p.Ala67Thr)	rs2151504209
NM_005861.4(STUB1):c.97G>A (p.Gly33Ser)	rs2039634238

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