List of variants in gene DPYD reported as likely benign for bone disorder

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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: 14

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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.2194G>A (p.Val732Ile)	rs1801160	0.03794
NM_000110.4(DPYD):c.*900T>C	rs17470762	0.02724
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.557A>G (p.Tyr186Cys)	rs115232898	0.00622
NM_000110.4(DPYD):c.1525-11G>A	rs55699321	0.00166
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.2766+19A>G	rs375268978	0.00056
NM_000110.4(DPYD):c.1524+16C>A	rs199469537	0.00048
NM_000110.4(DPYD):c.2303C>A (p.Thr768Lys)	rs56005131	0.00011
NM_000110.4(DPYD):c.45C>A (p.Ile15=)	rs267598790

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