List of variants in gene ATP1A3 reported as pathogenic for not provided

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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: 24

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HGVS	dbSNP	gnomAD frequency
NM_152296.5(ATP1A3):c.1838C>T (p.Thr613Met)
NM_152296.5(ATP1A3):c.2116G>A (p.Gly706Arg)	rs782175860
NM_152296.5(ATP1A3):c.2263G>T (p.Gly755Cys)	rs557052809
NM_152296.5(ATP1A3):c.2266C>T (p.Arg756Cys)	rs1064797245
NM_152296.5(ATP1A3):c.2267G>A (p.Arg756His)	rs606231435
NM_152296.5(ATP1A3):c.2318A>G (p.Asn773Ser)	rs606231437
NM_152296.5(ATP1A3):c.2324C>T (p.Pro775Leu)	rs886041396
NM_152296.5(ATP1A3):c.2401G>A (p.Asp801Asn)
NM_152296.5(ATP1A3):c.2443G>A (p.Glu815Lys)	rs387907281
NM_152296.5(ATP1A3):c.2452G>A (p.Glu818Lys)	rs587777771
NM_152296.5(ATP1A3):c.2600G>A (p.Gly867Asp)	rs606231442
NM_152296.5(ATP1A3):c.266G>C (p.Gly89Ala)	rs1599725621
NM_152296.5(ATP1A3):c.2677G>A (p.Gly893Arg)	rs1568853466
NM_152296.5(ATP1A3):c.2767G>A (p.Asp923Asn)	rs267606670
NM_152296.5(ATP1A3):c.2767G>T (p.Asp923Tyr)	rs267606670
NM_152296.5(ATP1A3):c.2806C>T (p.Gln936Ter)	rs1555859144
NM_152296.5(ATP1A3):c.2839G>A (p.Gly947Arg)	rs398122887
NM_152296.5(ATP1A3):c.2840G>A (p.Gly947Glu)	rs886041431
NM_152296.5(ATP1A3):c.3042A>C (p.Ter1014Cys)
NM_152296.5(ATP1A3):c.410C>T (p.Ser137Phe)	rs542652468
NM_152296.5(ATP1A3):c.967C>T (p.Pro323Ser)	rs864309572
NM_152296.5(ATP1A3):c.968C>T (p.Pro323Leu)	rs1085307933
NM_152296.5(ATP1A3):c.971A>G (p.Glu324Gly)	rs797044897
NM_152296.5(ATP1A3):c.974G>A (p.Gly325Asp)	rs863224847

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