ClinVar Miner

List of variants in gene MEGF10 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 104
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HGVS dbSNP gnomAD frequency
NM_001256545.2(MEGF10):c.3026-272A>G rs115469299 0.03322
NM_001256545.2(MEGF10):c.2981-165G>A rs41298322 0.03314
NM_001256545.2(MEGF10):c.3025+253A>G rs2270931 0.03312
NM_001256545.2(MEGF10):c.3233-299C>T rs17164929 0.03309
NM_001256545.2(MEGF10):c.3232+220C>G rs140094297 0.03297
NM_001256545.2(MEGF10):c.116+152G>A rs17684438 0.02654
NM_001256545.2(MEGF10):c.3233-176A>G rs17673727 0.02284
NM_001256545.2(MEGF10):c.1693+181G>A rs118151260 0.02169
NM_001256545.2(MEGF10):c.780+224C>T rs75840083 0.01815
NM_001256545.2(MEGF10):c.2105-103C>T rs76148405 0.01704
NM_001256545.2(MEGF10):c.918-80C>G rs80313631 0.01603
NM_001256545.2(MEGF10):c.918-148T>C rs77896531 0.01602
NM_001256545.2(MEGF10):c.1305+238_1305+239del rs3051621 0.01600
NM_001256545.2(MEGF10):c.-18-179A>G rs80220399 0.01434
NM_001256545.2(MEGF10):c.1590+262T>A rs74823398 0.01298
NM_001256545.2(MEGF10):c.1841-283T>C rs41298306 0.01223
NM_001256545.2(MEGF10):c.3232+40T>C rs116650470 0.01118
NM_001256545.2(MEGF10):c.780+240G>A rs75289329 0.01036
NM_001256545.2(MEGF10):c.413-328C>G rs116710294 0.01007
NM_001256545.2(MEGF10):c.219-30G>A rs79602606 0.00957
NM_001256545.2(MEGF10):c.-19+8943A>G rs79967765 0.00953
NM_001256545.2(MEGF10):c.2981-272A>G rs76912327 0.00939
NM_001256545.2(MEGF10):c.659+265A>G rs116312116 0.00886
NM_001256545.2(MEGF10):c.1975+260C>A rs141760181 0.00690
NM_001256545.2(MEGF10):c.412+135G>T rs143301955 0.00602
NM_001256545.2(MEGF10):c.1426+124G>A rs141134404 0.00570
NM_001256545.2(MEGF10):c.1591-89A>G rs73783791 0.00566
NM_001256545.2(MEGF10):c.117-172C>T rs79417344 0.00558
NM_001256545.2(MEGF10):c.413-267A>G rs76602283 0.00558
NM_001256545.2(MEGF10):c.1305+111C>G rs186226957 0.00553
NM_001256545.2(MEGF10):c.1130+206A>G rs75203304 0.00544
NM_001256545.2(MEGF10):c.1427-197T>A rs6889554 0.00509
NM_001256545.2(MEGF10):c.1590+114G>A rs150014181 0.00474
NM_001256545.2(MEGF10):c.2491+210T>A rs193147523 0.00427
NM_001256545.2(MEGF10):c.1975+60C>T rs139297404 0.00361
NM_001256545.2(MEGF10):c.659+153A>C rs150309123 0.00353
NM_001256545.2(MEGF10):c.2105-80T>C rs115371829 0.00349
NM_001256545.2(MEGF10):c.1694-278C>G rs115627422 0.00320
NM_001256545.2(MEGF10):c.2857-329A>G rs192760223 0.00308
NM_001256545.2(MEGF10):c.660-244T>C rs112696032 0.00304
NM_001256545.2(MEGF10):c.2491+303A>G rs185245474 0.00300
NM_001256545.2(MEGF10):c.303C>T (p.Ser101=) rs77203884 0.00260
NM_001256545.2(MEGF10):c.218+17C>G rs72786483 0.00257
NM_001256545.2(MEGF10):c.1002C>T (p.His334=) rs142947482 0.00254
NM_001256545.2(MEGF10):c.1500G>A (p.Gln500=) rs146075981 0.00243
NM_001256545.2(MEGF10):c.-18-11C>T rs138523651 0.00240
NM_001256545.2(MEGF10):c.*52G>T rs182533165 0.00235
NM_001256545.2(MEGF10):c.2463C>T (p.Pro821=) rs139929890 0.00229
NM_001256545.2(MEGF10):c.2654G>A (p.Gly885Glu) rs116500162 0.00227
NM_001256545.2(MEGF10):c.3003C>T (p.Ser1001=) rs35159176 0.00207
NM_001256545.2(MEGF10):c.1564G>A (p.Gly522Arg) rs140563851 0.00178
NM_001256545.2(MEGF10):c.1626C>T (p.Cys542=) rs146902993 0.00129
NM_001256545.2(MEGF10):c.2857-8T>G rs201148765 0.00117
NM_001256545.2(MEGF10):c.1602C>T (p.Tyr534=) rs114704569 0.00116
NM_001256545.2(MEGF10):c.3232+76T>C rs190980227 0.00116
NM_001256545.2(MEGF10):c.218+42G>A rs145752128 0.00098
NM_001256545.2(MEGF10):c.3026-8C>T rs185480820 0.00098
NM_001256545.2(MEGF10):c.1975+10G>A rs148814585 0.00080
NM_001256545.2(MEGF10):c.1130+3G>A rs115184652 0.00076
NM_001256545.2(MEGF10):c.-19+8927A>T rs573144174 0.00054
NM_001256545.2(MEGF10):c.1533C>T (p.Asp511=) rs151266058 0.00046
NM_001256545.2(MEGF10):c.1130+12C>T rs201836299 0.00032
NM_001256545.2(MEGF10):c.807C>T (p.Pro269=) rs146742773 0.00019
NM_001256545.2(MEGF10):c.2980+16G>A rs374003413 0.00017
NM_001256545.2(MEGF10):c.1839G>A (p.Arg613=) rs199930517 0.00011
NM_001256545.2(MEGF10):c.1130+13T>C rs746019129 0.00009
NM_001256545.2(MEGF10):c.2157T>C (p.His719=) rs374544972 0.00009
NM_001256545.2(MEGF10):c.2442T>C (p.Thr814=) rs370850456 0.00009
NM_001256545.2(MEGF10):c.2568C>T (p.Ile856=) rs778716392 0.00009
NM_001256545.2(MEGF10):c.2943G>A (p.Pro981=) rs371253627 0.00009
NM_001256545.2(MEGF10):c.120C>T (p.Tyr40=) rs372038844 0.00006
NM_001256545.2(MEGF10):c.1840+9C>G rs371418375 0.00006
NM_001256545.2(MEGF10):c.2104+7C>A rs371274853 0.00006
NM_001256545.2(MEGF10):c.3180A>G (p.Pro1060=) rs144450528 0.00005
NM_001256545.2(MEGF10):c.522G>A (p.Arg174=) rs201076330 0.00005
NM_001256545.2(MEGF10):c.3033A>T (p.Gly1011=) rs745591064 0.00004
NM_001256545.2(MEGF10):c.-7G>A rs4620069 0.00003
NM_001256545.2(MEGF10):c.917+6G>T rs746095070 0.00002
NM_001256545.2(MEGF10):c.-19+8977C>T rs559140741 0.00001
NM_001256545.2(MEGF10):c.1008C>T (p.Ser336=) rs145815113 0.00001
NM_001256545.2(MEGF10):c.116+12G>C rs775584154 0.00001
NM_001256545.2(MEGF10):c.1278A>G (p.Gly426=) rs139438683 0.00001
NM_001256545.2(MEGF10):c.2853G>A (p.Thr951=) rs966689979 0.00001
NM_001256545.2(MEGF10):c.2980+9T>C rs779077674 0.00001
NM_001256545.2(MEGF10):c.59T>C (p.Ile20Thr) rs748919606 0.00001
NM_001256545.2(MEGF10):c.930G>A (p.Glu310=) rs1264341592 0.00001
NM_001256545.2(MEGF10):c.-18-12dup rs774762160
NM_001256545.2(MEGF10):c.-19+8933A>G rs1057522065
NM_001256545.2(MEGF10):c.1673G>T (p.Arg558Leu) rs182243856
NM_001256545.2(MEGF10):c.174G>T (p.Thr58=) rs12654455
NM_001256545.2(MEGF10):c.2104+252C>T rs147085199
NM_001256545.2(MEGF10):c.2144C>A (p.Thr715Lys) rs147731088
NM_001256545.2(MEGF10):c.2729-279C>A rs2003863
NM_001256545.2(MEGF10):c.2729-279C>T rs2003863
NM_001256545.2(MEGF10):c.2980+249G>C rs41298316
NM_001256545.2(MEGF10):c.3026-273_3026-269del rs200590009
NM_001256545.2(MEGF10):c.3123G>A (p.Pro1041=) rs764182965
NM_001256545.2(MEGF10):c.320-134_320-130del rs141639621
NM_001256545.2(MEGF10):c.3215_3216delinsAC (p.Arg1072Asn) rs386692223
NM_001256545.2(MEGF10):c.412+127C>G rs115315224
NM_001256545.2(MEGF10):c.786A>G (p.Thr262=) rs893078096
NM_001256545.2(MEGF10):c.789G>T (p.Val263=) rs1188804374
NM_001256545.2(MEGF10):c.917+230dup rs112880381
NM_001256545.2(MEGF10):c.918-141G>C rs76221063

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