List of variants reported as uncertain significance for dihydropyrimidine dehydrogenase deficiency by Fulgent Genetics, Fulgent Genetics

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000110.4(DPYD):c.868A>G (p.Lys290Glu)	rs146356975	0.00078
NM_000110.4(DPYD):c.274C>G (p.Pro92Ala)	rs143986398	0.00013
NM_000110.4(DPYD):c.345G>C (p.Met115Ile)	rs377169736	0.00009
NM_000110.4(DPYD):c.2071G>T (p.Val691Leu)	rs202212118	0.00006
NM_000110.4(DPYD):c.2872A>G (p.Lys958Glu)	rs141044036	0.00006
NM_000110.4(DPYD):c.1796T>C (p.Met599Thr)	rs147601618	0.00003
NM_000110.4(DPYD):c.545T>A (p.Met182Lys)	rs779728902	0.00002
NM_000110.4(DPYD):c.2528T>C (p.Ile843Thr)	rs571114616	0.00001
NM_000110.4(DPYD):c.1349C>T (p.Ala450Val)	rs72975710

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