List of variants in gene combination ATP1A3, LOC130064543 reported as uncertain significance for autosomal dominant cerebellar ataxia

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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_152296.5(ATP1A3):c.-148T>G	rs769525784	0.00026
NM_152296.5(ATP1A3):c.-64A>G	rs373531937	0.00006
NM_152296.5(ATP1A3):c.-130GACG[3]	rs879996553

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