List of variants in gene MT-ND2 reported as uncertain significance by ClinGen Mitochondrial Disease Nuclear and Mitochondrial Variant Curation Expert Panel, ClinGen

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: 4

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND2):m.4735C>G	rs1603219589
NC_012920.1(MT-ND2):m.5001dup	rs1603219713
NC_012920.1(MT-ND2):m.5133_5134del	rs199476116
m.5244G>A	rs199476115

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