List of variants in gene DPYD reported as likely benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_000110.4(DPYD):c.1601G>A (p.Ser534Asn)	rs1801158	0.01380
NM_000110.4(DPYD):c.483+279C>A	rs79063448	0.01213
NM_000110.4(DPYD):c.2058+157G>A	rs115139529	0.00747
NM_000110.4(DPYD):c.775A>G (p.Lys259Glu)	rs45589337	0.00513
NM_000110.4(DPYD):c.484-145T>A	rs78682297	0.00477
NM_000110.4(DPYD):c.2908-208A>G	rs76665493	0.00437
NM_000110.4(DPYD):c.1128+161G>A	rs74105265	0.00414
NM_000110.4(DPYD):c.2180-3T>C	rs74104343	0.00158
NM_000110.4(DPYD):c.1701A>T (p.Gly567=)	rs148372305	0.00058
NM_000110.4(DPYD):c.2915A>G (p.Gln972Arg)	rs145529148	0.00054
NM_000110.4(DPYD):c.451A>G (p.Asn151Asp)	rs200562975	0.00049
NM_000110.4(DPYD):c.1905C>T (p.Asn635=)	rs3918289	0.00021
NM_000110.4(DPYD):c.525G>A (p.Ser175=)	rs6670886	0.00019
NM_000110.4(DPYD):c.258G>A (p.Pro86=)	rs201841475	0.00009
NM_000110.4(DPYD):c.1796T>C (p.Met599Thr)	rs147601618	0.00003
NM_000110.4(DPYD):c.2179+4A>G	rs746718279	0.00001
NM_000110.4(DPYD):c.2279C>T (p.Thr760Ile)	rs112766203	0.00001
NM_000110.4(DPYD):c.2299+7G>A	rs369672458	0.00001
NM_000110.4(DPYD):c.1020T>G (p.Ala340=)
NM_000110.4(DPYD):c.1617A>G (p.Gly539=)
NM_000110.4(DPYD):c.2223G>C (p.Leu741=)
NM_000110.4(DPYD):c.2442+69dup	rs544905665
NM_000110.4(DPYD):c.2623-8C>T	rs1570451084
NM_000110.4(DPYD):c.279T>C (p.Thr93=)	rs2101070143
NM_000110.4(DPYD):c.2994T>C (p.Ile998=)
NM_000110.4(DPYD):c.958+135dup	rs1397160848

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