ClinVar Miner

List of variants in gene CEP41 reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_018718.3(CEP41):c.574+294G>T rs7787084 0.52480
NM_018718.3(CEP41):c.-5A>C rs2287371 0.39010
NM_018718.3(CEP41):c.574+294del rs67842441 0.11792
NM_018718.3(CEP41):c.974-152_974-149dup rs71178583 0.09571
NC_000007.14:g.130441229dup rs150938510 0.09185
NM_018718.2(CEP41):c.-144G>A rs10230435 0.08654
NM_018718.3(CEP41):c.33+235A>G rs7784361 0.08441
NM_018718.3(CEP41):c.718T>G (p.Cys240Gly) rs113941736 0.00699
NM_018718.3(CEP41):c.208-5A>G rs11765434 0.00453
NM_018718.2(CEP41):c.-178C>T rs10230670
NM_018718.3(CEP41):c.33+142GCGGG[3] rs58073772
NM_018718.3(CEP41):c.574+295dup rs150874127
NM_018718.3(CEP41):c.575-14del rs144531086
NM_018718.3(CEP41):c.643-166A>C rs73484537
NM_018718.3(CEP41):c.97+220= rs6965346
NM_018718.3(CEP41):c.973+207_973+208dup rs34927892
NM_018718.3(CEP41):c.973+207dup rs34927892

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