ClinVar Miner

List of variants in gene CETP reported as likely benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_000078.3(CETP):c.118+270C>T rs5030708 0.01886
NM_000078.3(CETP):c.750+77G>A rs12720873 0.01854
NM_000078.3(CETP):c.982-177C>T rs8053613 0.01780
NM_000078.3(CETP):c.930+230A>G rs11644475 0.01633
NM_000078.3(CETP):c.66C>A (p.Thr22=) rs5884 0.01514
NM_000078.3(CETP):c.930+90G>A rs12691052 0.01489
NM_000078.3(CETP):c.982-119C>T rs34426213 0.01401
NM_000078.3(CETP):c.234-273G>T rs12708970 0.01337
NM_000078.3(CETP):c.658+132T>C rs12720925 0.01247
NM_000078.3(CETP):c.1322-72C>T rs36051594 0.00945
NM_000078.3(CETP):c.659-142C>T rs117040820 0.00836
NM_000078.3(CETP):c.460C>T (p.Arg154Trp) rs34716057 0.00764
NM_000078.3(CETP):c.1215-140G>A rs114948973 0.00691
NM_000078.3(CETP):c.1321+165A>G rs12720882 0.00644
NM_000078.3(CETP):c.119-215G>T rs59008849 0.00574
NM_000078.3(CETP):c.1146+187C>T rs12708979 0.00560
NM_000078.3(CETP):c.1214+152A>C rs140421500 0.00536
NM_000078.3(CETP):c.368+29T>C rs12708971 0.00518
NM_000078.3(CETP):c.118+51C>A rs34680782 0.00368
NM_000078.3(CETP):c.981+102A>G rs116351574 0.00348
NM_000078.3(CETP):c.233+227G>T rs192983539 0.00313
NM_000078.3(CETP):c.534G>A (p.Gly178=) rs34611098 0.00148
NM_000078.3(CETP):c.1153G>A (p.Val385Met) rs34855278 0.00108
NM_000078.3(CETP):c.921C>T (p.Asp307=) rs28381708 0.00079
NM_000078.3(CETP):c.1161C>T (p.Thr387=) rs7192120

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