ClinVar Miner

List of variants in gene MFN2 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_014874.4(MFN2):c.176-207G>A rs6675934 0.88297
NM_014874.4(MFN2):c.*58A>G rs1042842 0.71104
NM_014874.4(MFN2):c.474+65C>T rs2236056 0.64979
NM_014874.4(MFN2):c.1160+201C>G rs2236058 0.57223
NM_014874.4(MFN2):c.1873-66T>G rs7550536 0.54079
NM_014874.4(MFN2):c.816+260C>T rs2295281 0.45894
NM_014874.4(MFN2):c.1716+125C>T rs74052925 0.04600
NM_014874.4(MFN2):c.1716+91_1716+92dup rs150488282 0.04591
NM_014874.4(MFN2):c.1495+186A>G rs3766742 0.04496
NM_014874.4(MFN2):c.2069+82C>T rs11586204 0.04464
NM_014874.4(MFN2):c.600-25T>C rs41278626 0.04459
NM_014874.4(MFN2):c.1717-271A>G rs11579994 0.04446
NM_014874.4(MFN2):c.1039-22T>C rs6680984 0.04312
NM_014874.4(MFN2):c.1872+63T>C rs2273295 0.03984
NM_014874.4(MFN2):c.2070-63C>T rs115175952 0.03125
NM_014874.4(MFN2):c.1717-177T>C rs112638989 0.02858
NM_014874.4(MFN2):c.312-138C>G rs79244021 0.02852
NM_014874.4(MFN2):c.600-247G>A rs149142526 0.02659
NM_014874.4(MFN2):c.599+115A>C rs78727601 0.02499
NM_014874.4(MFN2):c.474+278A>G rs79492543 0.02496
NM_014874.4(MFN2):c.176-59C>G rs17037562 0.02488
NM_014874.4(MFN2):c.175+219_175+220del rs142734466 0.02485
NM_014874.4(MFN2):c.159C>T (p.Ser53=) rs61733200 0.02240
NM_014874.4(MFN2):c.2205-13C>A rs76020240 0.01362
NM_014874.4(MFN2):c.957C>T (p.Gly319=) rs41278632 0.00690
NM_014874.4(MFN2):c.2113G>A (p.Val705Ile) rs142271930 0.00621
NM_014874.4(MFN2):c.744C>T (p.Leu248=) rs61733205 0.00591
NM_014874.4(MFN2):c.1403G>A (p.Arg468His) rs138382758 0.00255
NM_014874.4(MFN2):c.892G>A (p.Gly298Arg) rs41278630 0.00221
NM_014874.4(MFN2):c.663T>C (p.Asp221=) rs116504054 0.00184
NM_014874.4(MFN2):c.1179G>A (p.Met393Ile) rs12069578 0.00153
NM_014874.4(MFN2):c.165C>T (p.Thr55=) rs77458527 0.00106
NM_014874.4(MFN2):c.408A>T (p.Val136=) rs78814413 0.00106
NM_014874.4(MFN2):c.150C>A (p.Ile50=) rs78841746 0.00089
NM_014874.4(MFN2):c.891C>T (p.Ala297=) rs11554508 0.00087
NM_014874.4(MFN2):c.1495+9C>T rs375494746 0.00059
NM_014874.4(MFN2):c.1827C>T (p.Ser609=) rs138724074 0.00039
NM_014874.4(MFN2):c.58C>T (p.His20Tyr) rs201715603 0.00004
NM_014874.4(MFN2):c.1806C>T (p.Ser602=) rs201258935 0.00001
NM_014874.4(MFN2):c.-149-43_-149-38dup rs34602102
NM_014874.4(MFN2):c.-149-44_-149-38dup rs34602102
NM_014874.4(MFN2):c.-149-45_-149-38dup rs34602102
NM_014874.4(MFN2):c.1161-312del rs60299433
NM_014874.4(MFN2):c.1161-312dup rs60299433
NM_014874.4(MFN2):c.1716+233dup rs3830887
NM_014874.4(MFN2):c.1873-154C>G rs116069423
NM_014874.4(MFN2):c.2205-120C>G rs3766741
NM_014874.4(MFN2):c.311+285_311+289dup rs35911686
NM_014874.4(MFN2):c.311+286_311+289dup rs35911686
NM_014874.4(MFN2):c.311+287_311+289dup rs35911686
NM_014874.4(MFN2):c.311+289dup rs35911686
NM_014874.4(MFN2):c.475-240del rs35141271
NM_014874.4(MFN2):c.475-241_475-240del rs35141271
NM_014874.4(MFN2):c.600-220AAAAC[4] rs55676620

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