Variants in gene PHGDH with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_006623.4(PHGDH):c.318C>T (p.Ala106=)	rs115747918	0.01251
NM_006623.4(PHGDH):c.792+6T>G	rs146953046	0.01118
NM_006623.4(PHGDH):c.595C>G (p.Leu199Val)	rs77632964	0.00622
NM_006623.4(PHGDH):c.624T>C (p.Pro208=)	rs77401816	0.00154
NM_006623.4(PHGDH):c.510+6A>G	rs371736796	0.00133
NM_006623.4(PHGDH):c.1559C>A (p.Ala520Glu)	rs151275800	0.00101
NM_006623.4(PHGDH):c.985A>T (p.Thr329Ser)	rs201298102	0.00064
NM_006623.4(PHGDH):c.1257G>A (p.Gly419=)	rs374303746	0.00016
NM_006623.4(PHGDH):c.1116C>T (p.Pro372=)	rs587662790	0.00004
NM_006623.4(PHGDH):c.519G>A (p.Gly173=)	rs754326499

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