Variants in gene PHKA2 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000292.3(PHKA2):c.1246G>A (p.Gly416Arg)	rs16980929	0.00485
NM_000292.3(PHKA2):c.1670C>G (p.Thr557Arg)	rs201183167	0.00038

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