List of variants in gene combination LOC129929423, MFN2 reported as uncertain significance 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_014874.3(MFN2):c.-359C>G	rs997846275	0.00049
NM_014874.3(MFN2):c.-382G>A	rs568548916	0.00047
NM_014874.3(MFN2):c.-468G>A	rs973376897	0.00006
NM_014874.3(MFN2):c.-328T>A	rs886045217	0.00005
NM_014874.3(MFN2):c.-344C>T	rs886045216

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