Variants in gene ATP1A3 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_152296.5(ATP1A3):c.1825G>T (p.Asp609Tyr)
NM_152296.5(ATP1A3):c.2116G>A (p.Gly706Arg)	rs782175860
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.2324C>T (p.Pro775Leu)	rs886041396
NM_152296.5(ATP1A3):c.266G>C (p.Gly89Ala)	rs1599725621
NM_152296.5(ATP1A3):c.385G>A (p.Val129Met)	rs1555865401
NM_152296.5(ATP1A3):c.829G>A (p.Glu277Lys)	rs80356533

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