ClinVar Miner

List of variants in gene ELAC2 reported as benign for not provided

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Gene type:
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Total variants: 76
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HGVS dbSNP gnomAD frequency
NM_018127.6(ELAC2):c.-381A>G rs2051974 0.70622
NM_018127.7(ELAC2):c.*206C>T rs1044569 0.57710
NM_018127.7(ELAC2):c.*320G>A rs2523 0.56964
NM_018127.7(ELAC2):c.*151C>G rs1044564 0.56298
NM_018127.7(ELAC2):c.2254-191G>A rs9908102 0.55172
NM_018127.6(ELAC2):c.-408C>T rs2051973 0.51780
NM_018127.7(ELAC2):c.2109-145T>G rs9915058 0.51544
NM_018127.7(ELAC2):c.1305-8T>C rs3760316 0.32355
NM_018127.7(ELAC2):c.433-241G>A rs733890 0.29579
NM_018127.7(ELAC2):c.1080-326T>C rs58842254 0.28406
NM_018127.7(ELAC2):c.739-208C>T rs111859801 0.28104
NM_018127.7(ELAC2):c.679+185C>G rs73300518 0.27910
NM_018127.7(ELAC2):c.490+277T>C rs7211501 0.27756
NM_018127.7(ELAC2):c.679+60T>C rs41494747 0.27742
NM_018127.7(ELAC2):c.433-305T>C rs733889 0.27728
NM_018127.7(ELAC2):c.679+146T>G rs73981622 0.27713
NM_018127.7(ELAC2):c.650C>T (p.Ser217Leu) rs4792311 0.27559
NM_018127.7(ELAC2):c.297-11T>C rs58809197 0.27292
NM_018127.7(ELAC2):c.984-204C>G rs58578352 0.27005
NM_018127.7(ELAC2):c.1423+239C>T rs55787925 0.26969
NM_018127.7(ELAC2):c.1218+15C>T rs55825263 0.26965
NM_018127.7(ELAC2):c.1304+17A>T rs55674356 0.26960
NM_018127.7(ELAC2):c.871-316A>T rs4792310 0.26960
NM_018127.7(ELAC2):c.1423+308C>T rs55986816 0.26951
NM_018127.7(ELAC2):c.1305-337G>A rs73981608 0.26901
NM_018127.7(ELAC2):c.1808+233G>C rs2286340 0.26491
NM_018127.7(ELAC2):c.433-296T>C rs4792312 0.19098
NC_000017.11:g.13018395G>C rs17554679 0.10755
NM_018127.7(ELAC2):c.680-36A>G rs2302069 0.10233
NM_018127.7(ELAC2):c.490+206G>A rs138536836 0.09206
NM_018127.7(ELAC2):c.491-253del rs61296396 0.08989
NM_018127.7(ELAC2):c.1893A>G (p.Thr631=) rs17552022 0.08581
NM_018127.7(ELAC2):c.491-14T>C rs74556312 0.08556
NM_018127.7(ELAC2):c.433-43C>T rs56004910 0.08523
NM_018127.7(ELAC2):c.983+59A>T rs17639379 0.08522
NM_018127.7(ELAC2):c.491-170T>G rs76738579 0.08521
NM_018127.7(ELAC2):c.559+136G>A rs74886662 0.08519
NM_018127.7(ELAC2):c.2253+171C>G rs74937316 0.08518
NM_018127.7(ELAC2):c.2108+73G>A rs56329828 0.08506
NM_018127.7(ELAC2):c.2254-211G>A rs76491525 0.08503
NM_018127.7(ELAC2):c.984-132C>T rs77703211 0.08503
NM_018127.7(ELAC2):c.738+241G>A rs138505842 0.08498
NM_018127.7(ELAC2):c.1305-225G>A rs75426043 0.08496
NM_018127.7(ELAC2):c.1520+41C>T rs56405144 0.08486
NM_018127.7(ELAC2):c.432+105C>T rs10521207 0.04805
NM_018127.7(ELAC2):c.798-20G>T rs77528900 0.03735
NM_018127.7(ELAC2):c.1621G>A (p.Ala541Thr) rs5030739 0.02886
NM_018127.7(ELAC2):c.2130C>T (p.Ser710=) rs7217826 0.02093
NM_018127.7(ELAC2):c.1389C>T (p.Tyr463=) rs77972324 0.01451
NM_018127.7(ELAC2):c.1479G>C (p.Pro493=) rs140335642 0.00771
NM_018127.7(ELAC2):c.368-4T>A rs139778647 0.00657
NM_018127.7(ELAC2):c.560-2A>G rs149733287 0.00275
NM_018127.7(ELAC2):c.174G>A (p.Val58=) rs2286334 0.00196
NM_018127.7(ELAC2):c.1390A>T (p.Arg464Trp) rs200149324 0.00026
NC_000017.11:g.13018031G>C rs4792315
NM_018127.7(ELAC2):c.*280T>A rs6949
NM_018127.7(ELAC2):c.1079+72G>C rs59429173
NM_018127.7(ELAC2):c.1080-236del rs137953448
NM_018127.7(ELAC2):c.1304+65del rs56341811
NM_018127.7(ELAC2):c.1424-284C>A rs80003444
NM_018127.7(ELAC2):c.1520+182dup rs11443554
NM_018127.7(ELAC2):c.1521-258del rs57024446
NM_018127.7(ELAC2):c.1560A>G (p.Thr520=) rs11545302
NM_018127.7(ELAC2):c.1659+138T>C rs4792308
NM_018127.7(ELAC2):c.1808+229T>C rs80068662
NM_018127.7(ELAC2):c.1808+26G>C rs2286338
NM_018127.7(ELAC2):c.1809-252C>T rs73981605
NM_018127.7(ELAC2):c.1809-75G>T rs73981604
NM_018127.7(ELAC2):c.367+116del rs879009279
NM_018127.7(ELAC2):c.367+117G>T rs1322267627
NM_018127.7(ELAC2):c.367+95dup rs879009279
NM_018127.7(ELAC2):c.679+148G>A rs73981621
NM_018127.7(ELAC2):c.871-188_871-183del rs10532461
NM_018127.7(ELAC2):c.983+102A>G rs4792309
NM_018127.7(ELAC2):c.984-237T>C rs58700278
NM_018127.7(ELAC2):c.984-237T>G rs58700278

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