List of variants in gene ATXN10 reported as uncertain significance for cerebellar disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_013236.4(ATXN10):c.404G>T (p.Gly135Val)	rs199766375	0.00016
NM_013236.4(ATXN10):c.13A>G (p.Arg5Gly)	rs1296770412	0.00001
NM_013236.4(ATXN10):c.1165C>T (p.Gln389Ter)
NM_013236.4(ATXN10):c.647+1G>A

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