ClinVar Miner

List of variants reported as likely benign for dihydropyrimidine dehydrogenase deficiency by Genome-Nilou Lab

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_000110.4(DPYD):c.681-8C>T rs74774246 0.01331
NM_000110.4(DPYD):c.1371C>T (p.Asn457=) rs57918000 0.00785
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.1524+16C>A rs199469537 0.00048

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