List of variants in gene combination ATP1A3, LOC130064543 reported as likely benign for Dystonia 12

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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_152296.5(ATP1A3):c.6+3A>G	rs369853936	0.00016
NM_152296.5(ATP1A3):c.6+17C>A	rs782567963	0.00001
NM_152296.5(ATP1A3):c.6+14C>G
NM_152296.5(ATP1A3):c.6+7G>A	rs2145995390

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