List of variants in gene combination LOC129929426, MFN2 reported as likely benign for Charcot-Marie-Tooth disease type 2

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_014874.4(MFN2):c.1677C>T (p.Pro559=)	rs1219420062	0.00001
NM_014874.4(MFN2):c.1716+8A>G	rs1639390139	0.00001
NM_014874.4(MFN2):c.1686C>T (p.Ser562=)	rs1210577569
NM_014874.4(MFN2):c.1689T>C (p.Arg563=)	rs2523088767
NM_014874.4(MFN2):c.1716+10G>C
NM_014874.4(MFN2):c.1716+16C>A	rs2100853696
NM_014874.4(MFN2):c.1716+16C>T	rs2100853696
NM_014874.4(MFN2):c.1716+19C>A	rs2523089345

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