ClinVar Miner

List of variants in gene MEGF10 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_001256545.2(MEGF10):c.*209C>G rs10793809 0.74642
NM_001256545.2(MEGF10):c.-19+8919G>C rs1345662 0.53810
NM_001256545.2(MEGF10):c.117-199A>G rs27782 0.39893
NM_001256545.2(MEGF10):c.-122G>A rs2032834 0.38334
NM_001256545.2(MEGF10):c.781-197A>C rs11952552 0.23313
NM_001256545.2(MEGF10):c.1130+141G>A rs3851469 0.22488
NM_001256545.2(MEGF10):c.2105-272A>C rs2408871 0.20278
NM_001256545.2(MEGF10):c.660-101A>G rs6595767 0.19743
NM_001256545.2(MEGF10):c.3026-252T>G rs72790443 0.13645
NM_001256545.2(MEGF10):c.2728+61T>C rs2270933 0.12698
NM_001256545.2(MEGF10):c.3233-58T>C rs3812053 0.10922
NM_001256545.2(MEGF10):c.659+302T>G rs72788599 0.10637
NM_001256545.2(MEGF10):c.2362+64T>G rs41298308 0.10584
NM_001256545.2(MEGF10):c.660-73C>T rs6595768 0.10504
NM_001256545.2(MEGF10):c.3026-125A>T rs72790444 0.10326
NM_001256545.2(MEGF10):c.1975+43C>T rs72790419 0.10318
NM_001256545.2(MEGF10):c.2728+183G>A rs41298312 0.10041
NM_001256545.2(MEGF10):c.2234-124T>C rs60681812 0.09602
NM_001256545.2(MEGF10):c.1590+296G>C rs17673517 0.09463
NM_001256545.2(MEGF10):c.319+232A>G rs17165041 0.08751
NM_001256545.2(MEGF10):c.2856+181C>A rs58718502 0.07469
NM_001256545.2(MEGF10):c.2491+32C>T rs7737871 0.05291
NM_001256545.2(MEGF10):c.319+206T>C rs17839697 0.04973
NM_001256545.2(MEGF10):c.218+155G>A rs17673170 0.04936
NM_001256545.2(MEGF10):c.2105-322G>T rs73783795 0.04589
NM_001256545.2(MEGF10):c.218+188G>C rs57261222 0.01609
NM_001256545.2(MEGF10):c.609C>T (p.Cys203=) rs113794264 0.00845
NM_001256545.2(MEGF10):c.*4C>G rs73783802 0.00588
NM_001256545.2(MEGF10):c.1046G>A (p.Arg349His) rs78847357 0.00577
NM_001256545.2(MEGF10):c.117-5_117-4insC rs538399152 0.00081
NM_001256545.2(MEGF10):c.-19+8702del rs35796097
NM_001256545.2(MEGF10):c.1131-280C>A rs79655685
NM_001256545.2(MEGF10):c.1306-278dup rs111958224
NM_001256545.2(MEGF10):c.1975+96_1975+118del rs11273003
NM_001256545.2(MEGF10):c.2104+163del rs573923853
NM_001256545.2(MEGF10):c.219-333GA[3] rs147858479
NM_001256545.2(MEGF10):c.2857-292del rs199921206
NM_001256545.2(MEGF10):c.2857-292dup rs199921206
NM_001256545.2(MEGF10):c.3232+117TATTT[7] rs58939267
NM_001256545.2(MEGF10):c.412+226G>A rs1422318

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