List of variants in gene MFN2 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_014874.4(MFN2):c.892G>A (p.Gly298Arg)	rs41278630	0.00221
NM_014874.4(MFN2):c.72G>T (p.Val24=)	rs138454088	0.00044
NM_014874.4(MFN2):c.474+4A>G	rs141974160	0.00014
NM_014874.4(MFN2):c.870C>T (p.Gly290=)	rs368302487	0.00014
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.2145C>T (p.Ala715=)	rs571011689	0.00003
NM_014874.4(MFN2):c.1605T>C (p.Ala535=)	rs575884069	0.00001
NM_014874.4(MFN2):c.1815C>T (p.Thr605=)	rs751029047	0.00001
NM_014874.4(MFN2):c.1155G>A (p.Glu385=)
NM_014874.4(MFN2):c.1458C>T (p.Ile486=)
NM_014874.4(MFN2):c.1717-9_1717-6del	rs746359726
NM_014874.4(MFN2):c.1980C>T (p.Ala660=)	rs2100858469
NM_014874.4(MFN2):c.474+6G>A

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