ClinVar Miner

List of variants in gene MFN2 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_014874.4(MFN2):c.817-108G>A rs139807696 0.02523
NM_014874.4(MFN2):c.2069+30G>C rs77941748 0.01637
NM_014874.4(MFN2):c.475-232T>G rs115256192 0.01616
NM_014874.3(MFN2):c.-249T>A rs2180182 0.01549
NM_014874.3(MFN2):c.-287C>T rs2180181 0.01549
NM_014874.4(MFN2):c.2204+118A>G rs77738831 0.01480
NM_014874.4(MFN2):c.1495+310C>T rs116817317 0.01457
NM_014874.4(MFN2):c.1039-41C>G rs115054993 0.01366
NM_014874.4(MFN2):c.1496-34T>C rs143065633 0.01190
NM_014874.4(MFN2):c.474+86A>C rs6678781 0.01151
NM_014874.4(MFN2):c.600-116G>A rs41278624 0.00928
NM_014874.4(MFN2):c.599+109A>G rs75754772 0.00898
NM_014874.4(MFN2):c.176-200G>T rs116722569 0.00844
NM_014874.4(MFN2):c.-4-221C>A rs192381474 0.00799
NM_014874.4(MFN2):c.311+315A>G rs114350897 0.00670
NM_014874.4(MFN2):c.475-38T>C rs151226551 0.00556
NM_014874.4(MFN2):c.1495+236C>A rs141359660 0.00479
NM_014874.4(MFN2):c.474+88G>C rs540377814 0.00302
NM_014874.4(MFN2):c.1403G>A (p.Arg468His) rs138382758 0.00255
NM_014874.4(MFN2):c.1161-197C>T rs117745744 0.00247
NM_014874.4(MFN2):c.892G>A (p.Gly298Arg) rs41278630 0.00221
NM_014874.4(MFN2):c.475-33C>T rs76051569 0.00168
NM_014874.4(MFN2):c.1179G>A (p.Met393Ile) rs12069578 0.00153
NM_014874.4(MFN2):c.-4-13G>T rs373679523 0.00060
NM_014874.4(MFN2):c.1495+9C>T rs375494746 0.00059
NM_014874.4(MFN2):c.72G>T (p.Val24=) rs138454088 0.00044
NM_014874.4(MFN2):c.1728C>T (p.Pro576=) rs147802404 0.00036
NM_014874.4(MFN2):c.2146G>A (p.Ala716Thr) rs144860227 0.00032
NM_014874.4(MFN2):c.971-16A>G rs374822911 0.00019
NM_014874.4(MFN2):c.175+9G>A rs373340717 0.00018
NM_014874.4(MFN2):c.2157G>A (p.Lys719=) rs148441213 0.00017
NM_014874.4(MFN2):c.444C>T (p.Thr148=) rs373038884 0.00017
NM_014874.4(MFN2):c.2069+16G>A rs376673392 0.00016
NM_014874.4(MFN2):c.-161G>A rs140094248 0.00014
NM_014874.4(MFN2):c.870C>T (p.Gly290=) rs368302487 0.00014
NM_014874.4(MFN2):c.1476C>A (p.Thr492=) rs143428548 0.00013
NM_014874.4(MFN2):c.2112C>T (p.Asp704=) rs374371748 0.00010
NM_014874.4(MFN2):c.160G>A (p.Ala54Thr) rs61733203 0.00008
NM_014874.4(MFN2):c.1617A>G (p.Glu539=) rs556515947 0.00007
NM_014874.4(MFN2):c.1779G>A (p.Ser593=) rs367623682 0.00006
NM_014874.4(MFN2):c.1875G>A (p.Val625=) rs747719940 0.00006
NM_014874.4(MFN2):c.-10A>G rs575581303 0.00004
NM_014874.4(MFN2):c.1529G>A (p.Arg510Gln) rs376598131 0.00004
NM_014874.4(MFN2):c.176-7C>T rs374055101 0.00004
NM_014874.4(MFN2):c.2069+15C>T rs375924621 0.00004
NM_014874.4(MFN2):c.522T>C (p.His174=) rs762789747 0.00004
NM_014874.4(MFN2):c.1113G>A (p.Ala371=) rs766570486 0.00003
NM_014874.4(MFN2):c.1161-18C>T rs1351551038 0.00003
NM_014874.4(MFN2):c.204C>T (p.Pro68=) rs148399574 0.00003
NM_014874.4(MFN2):c.1873-4G>C rs369338141 0.00002
NM_014874.4(MFN2):c.311+9T>C rs771439230 0.00002
NM_014874.4(MFN2):c.645G>A (p.Lys215=) rs767693664 0.00002
NM_014874.4(MFN2):c.696C>G (p.Thr232=) rs769923700 0.00002
NM_014874.4(MFN2):c.1039-20C>T rs1253046105 0.00001
NM_014874.4(MFN2):c.1293G>T (p.Ser431=) rs751915674 0.00001
NM_014874.4(MFN2):c.1413G>A (p.Glu471=) rs745360979 0.00001
NM_014874.4(MFN2):c.311+8C>T rs747730092 0.00001
NM_014874.4(MFN2):c.312-19A>G rs756393202 0.00001
NM_014874.4(MFN2):c.525C>T (p.Ala175=) rs751505990 0.00001
NM_014874.4(MFN2):c.-149-20C>A rs1053095330
NM_014874.4(MFN2):c.-149-46_-149-45insGTTTTTTTTT rs763918741
NM_014874.4(MFN2):c.171T>C (p.Leu57=) rs1443899568
NM_014874.4(MFN2):c.1920C>G (p.Leu640=) rs141468012
NM_014874.4(MFN2):c.1968C>G (p.Ala656=) rs763381681
NM_014874.4(MFN2):c.2026G>A (p.Val676Ile) rs1057520619
NM_014874.4(MFN2):c.311+288_311+289dup rs35911686
NM_014874.4(MFN2):c.475-240dup rs35141271
NM_014874.4(MFN2):c.475-259C>A rs1425252988
NM_014874.4(MFN2):c.564C>T (p.Cys188=) rs536007087
NM_014874.4(MFN2):c.666G>A (p.Val222=) rs911933291
NM_014874.4(MFN2):c.927G>C (p.Val309=) rs779947209

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