ClinVar Miner

List of variants in gene DICER1 reported as benign by Breakthrough Genomics, Breakthrough Genomics

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_177438.3(DICER1):c.*1630G>A rs1187652 0.97929
NM_177438.3(DICER1):c.*88T>A rs13078 0.85229
NM_177438.3(DICER1):c.734+155A>G rs11620843 0.41751
NM_177438.3(DICER1):c.4206+9G>T rs1778057 0.26377
NM_177438.3(DICER1):c.*2693A>G rs1057035 0.25588
NM_177438.3(DICER1):c.2041-91A>G rs2297730 0.18396
NM_177438.3(DICER1):c.573+116C>T rs1953535 0.10094
NM_177438.3(DICER1):c.*3473T>C rs3742330 0.09263
NM_177438.3(DICER1):c.904-65C>T rs67737119 0.08726
NM_177438.3(DICER1):c.1907+43C>T rs11624081 0.06928
NM_177438.3(DICER1):c.2117-63A>C rs17091823 0.03717
NM_177438.3(DICER1):c.4680G>A (p.Ala1560=) rs61729797 0.03654
NM_177438.3(DICER1):c.1908-77C>T rs57681406 0.03390
NM_177438.3(DICER1):c.3033G>A (p.Ala1011=) rs8019857 0.03377
NM_177438.3(DICER1):c.5096-132T>C rs1006157 0.03373
NM_177438.3(DICER1):c.2437-113A>T rs57932364 0.03006
NM_177438.3(DICER1):c.*433G>T rs10144436 0.03002
NM_177438.3(DICER1):c.3198T>C (p.Thr1066=) rs114964211 0.01414
NM_177438.3(DICER1):c.2370G>A (p.Arg790=) rs112712209 0.00732
NM_177438.3(DICER1):c.*873G>A rs45518832 0.00615
NM_177438.3(DICER1):c.*1575A>G rs190465278 0.00406
NM_177438.3(DICER1):c.735-74G>T rs79285101

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