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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001931.5(DLAT):c.165C>G (p.Val55=)	rs199520186	0.00006
NM_001931.5(DLAT):c.583C>T (p.Pro195Ser)	rs149440666	0.00006
NM_001931.5(DLAT):c.423G>A (p.Glu141=)	rs781936816	0.00001

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