List of variants in gene combination ATXN1, LOC108663993 reported as uncertain significance for cerebellar degeneration

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001128164.2(ATXN1):c.630G>T (p.Gln210His)	rs368218879	0.00014
NM_001128164.2(ATXN1):c.636G>T (p.Gln212His)	rs376233432	0.00010
NM_001128164.2(ATXN1):c.641_642insTCAGCA (p.Gln213_Gln214insHisGln)

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