Variants in gene PHKA2 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (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_000292.3(PHKA2):c.4C>G (p.Arg2Gly)	rs140014925	0.00005
NM_000292.3(PHKA2):c.133C>T (p.Arg45Trp)	rs1601781031
NM_000292.3(PHKA2):c.134G>A (p.Arg45Gln)	rs1601781024
NM_000292.3(PHKA2):c.2746C>T (p.Arg916Trp)	rs1569297427
NM_000292.3(PHKA2):c.3210_3212del (p.Arg1072del)	rs1555989523
NM_000292.3(PHKA2):c.3629G>A (p.Gly1210Glu)	rs1601685358
NM_000292.3(PHKA2):c.884G>A (p.Arg295His)	rs797044877
NM_000292.3(PHKA2):c.892C>T (p.Arg298Ter)	rs2518766696

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