List of variants in gene MFN2 reported as likely pathogenic by Inherited Neuropathy Consortium

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_014874.4(MFN2):c.272T>G (p.Val91Gly)	rs1569816262
NM_014874.4(MFN2):c.475-2A>G	rs1557522794
NM_014874.4(MFN2):c.572T>C (p.Leu191Pro)	rs879254288

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