List of variants in gene DPYD reported as benign by Athena Diagnostics Inc

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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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.2194G>A (p.Val732Ile)	rs1801160	0.03794
NM_000110.4(DPYD):c.1218G>A (p.Met406Ile)	rs61622928	0.02183
NM_000110.4(DPYD):c.681-8C>T	rs74774246	0.01331
NM_000110.4(DPYD):c.1236G>A (p.Glu412=)	rs56038477	0.01297
NM_000110.4(DPYD):c.1371C>T (p.Asn457=)	rs57918000	0.00785
NM_000110.4(DPYD):c.483+601C>G	rs72977734	0.00584
NM_000110.4(DPYD):c.2180-3T>C	rs74104343	0.00158
NM_000110.4(DPYD):c.3067C>A (p.Pro1023Thr)	rs114096998

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