List of variants in gene MFN2 reported as benign by Athena Diagnostics Inc

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_014874.4(MFN2):c.159C>T (p.Ser53=)	rs61733200	0.02240
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.663T>C (p.Asp221=)	rs116504054	0.00184
NM_014874.4(MFN2):c.1179G>A (p.Met393Ile)	rs12069578	0.00153
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.1827C>T (p.Ser609=)	rs138724074	0.00039

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