List of variants in gene MFN2 reported as benign for Charcot-Marie-Tooth disease

Minimum submission review status:		Collection method:
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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
NM_014874.3(MFN2):c.1039-19G>A	rs74052923
NM_014874.3(MFN2):c.1179G>A (p.Met393Ile)	rs12069578
NM_014874.3(MFN2):c.1495+9C>T	rs375494746
NM_014874.3(MFN2):c.1569C>T (p.Ser523=)	rs1042837
NM_014874.3(MFN2):c.159C>T (p.Ser53=)	rs61733200
NM_014874.3(MFN2):c.2113G>A (p.Val705Ile)	rs142271930
NM_014874.3(MFN2):c.2204+15T>C	rs77262016
NM_014874.3(MFN2):c.2205-13C>A	rs76020240
NM_014874.3(MFN2):c.744C>T (p.Leu248=)	rs61733205
NM_014874.3(MFN2):c.957C>T (p.Gly319=)	rs41278632
NM_014874.3(MFN2):c.970+19G>A	rs75865135

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