Variants in gene DPYD 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000110.4(DPYD):c.496A>G (p.Met166Val)	rs2297595	0.08071
NM_000110.4(DPYD):c.557A>G (p.Tyr186Cys)	rs115232898	0.00622
NM_000110.4(DPYD):c.2303C>A (p.Thr768Lys)	rs56005131	0.00011
NM_000110.4(DPYD):c.1796T>C (p.Met599Thr)	rs147601618	0.00003

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