Variants in gene PHGDH with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (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: 4

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HGVS	dbSNP	gnomAD frequency
NM_006623.4(PHGDH):c.1559C>A (p.Ala520Glu)	rs151275800	0.00101
NM_006623.4(PHGDH):c.834C>A (p.Val278=)	rs147866831	0.00051
NM_006623.4(PHGDH):c.1257G>A (p.Gly419=)	rs374303746	0.00016
NM_006623.4(PHGDH):c.519G>A (p.Gly173=)	rs754326499

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