Variants in gene DPYD with conflicting interpretations "benign" and "drug response"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (drug response) minimum review status:		Submission 2 (drug response) 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000110.4(DPYD):c.85T>C (p.Cys29Arg)	rs1801265	0.27966
NM_000110.4(DPYD):c.1627A>G (p.Ile543Val)	rs1801159	0.18679
NM_000110.4(DPYD):c.496A>G (p.Met166Val)	rs2297595	0.08071
NM_000110.4(DPYD):c.1896T>C (p.Phe632=)	rs17376848	0.04278
NM_000110.4(DPYD):c.2194G>A (p.Val732Ile)	rs1801160	0.03794
NM_000110.4(DPYD):c.1601G>A (p.Ser534Asn)	rs1801158	0.01380
NM_000110.4(DPYD):c.1236G>A (p.Glu412=)	rs56038477	0.01297
NM_000110.4(DPYD):c.1129-5923C>G	rs75017182	0.01296
NM_000110.4(DPYD):c.2846A>T (p.Asp949Val)	rs67376798	0.00334

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