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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_014874.4(MFN2):c.*58A>G	rs1042842	0.71104
NM_014874.4(MFN2):c.2204+15T>C	rs77262016	0.07571
NM_014874.4(MFN2):c.1569C>T (p.Ser523=)	rs1042837	0.04459
NM_014874.4(MFN2):c.-149-15T>G	rs114306601	0.02587
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.1039-19G>A	rs74052923	0.01120
NM_014874.4(MFN2):c.970+19G>A	rs75865135	0.00707
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.975C>T (p.Gly325=)	rs141475476	0.00357
NM_014874.4(MFN2):c.*15G>A	rs141339523	0.00292
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.1452G>A (p.Thr484=)	rs150043585	0.00083
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.1779G>A (p.Ser593=)	rs367623682	0.00006
NM_014874.4(MFN2):c.1806C>T (p.Ser602=)	rs201258935	0.00001
NM_014874.4(MFN2):c.1717-9_1717-6del	rs746359726

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