ClinVar Miner

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

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Gene type:
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Total variants: 64
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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.957C>T (p.Gly319=) rs41278632 0.00690
NM_014874.4(MFN2):c.311+315A>G rs114350897 0.00670
NM_014874.4(MFN2):c.2113G>A (p.Val705Ile) rs142271930 0.00621
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.663T>C (p.Asp221=) rs116504054 0.00184
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.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.1452G>A (p.Thr484=) rs150043585 0.00083
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.756C>T (p.Asn252=) rs137960129 0.00053
NM_014874.4(MFN2):c.1827C>T (p.Ser609=) rs138724074 0.00039
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.2157G>A (p.Lys719=) rs148441213 0.00017
NM_014874.4(MFN2):c.444C>T (p.Thr148=) rs373038884 0.00017
NM_014874.4(MFN2):c.870C>T (p.Gly290=) rs368302487 0.00014
NM_014874.4(MFN2):c.160G>A (p.Ala54Thr) rs61733203 0.00008
NM_014874.4(MFN2):c.1779G>A (p.Ser593=) rs367623682 0.00006
NM_014874.4(MFN2):c.1529G>A (p.Arg510Gln) rs376598131 0.00004
NM_014874.4(MFN2):c.522T>C (p.His174=) rs762789747 0.00004
NM_014874.4(MFN2):c.1146G>A (p.Ala382=) rs752630853 0.00003
NM_014874.4(MFN2):c.1161-18C>T rs1351551038 0.00003
NM_014874.4(MFN2):c.119A>G (p.Asn40Ser) rs1354203259 0.00003
NM_014874.4(MFN2):c.204C>T (p.Pro68=) rs148399574 0.00003
NM_014874.4(MFN2):c.645G>A (p.Lys215=) rs767693664 0.00002
NM_014874.4(MFN2):c.1413G>A (p.Glu471=) rs745360979 0.00001
NM_014874.4(MFN2):c.1824C>T (p.Ala608=) rs774988978 0.00001
NM_014874.4(MFN2):c.525C>T (p.Ala175=) rs751505990 0.00001
NM_014874.4(MFN2):c.-149-46_-149-45insGTTTTTTTTT rs763918741
NM_014874.4(MFN2):c.1161-234C>T
NM_014874.4(MFN2):c.147C>T (p.Tyr49=)
NM_014874.4(MFN2):c.1717-9_1717-6del rs746359726
NM_014874.4(MFN2):c.1920C>G (p.Leu640=) rs141468012
NM_014874.4(MFN2):c.1935C>T (p.Tyr645=)
NM_014874.4(MFN2):c.311+288_311+289dup rs35911686
NM_014874.4(MFN2):c.475-10C>G rs2100825982
NM_014874.4(MFN2):c.475-240dup rs35141271
NM_014874.4(MFN2):c.475-259C>A rs1425252988
NM_014874.4(MFN2):c.927G>C (p.Val309=) rs779947209
NM_014874.4(MFN2):c.930C>T (p.Leu310=) rs1569852141

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