List of variants in gene MT-ND1 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: 7

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND1):m.3357G>C	rs1556422714
NC_012920.1(MT-ND1):m.3502T>C	rs1603218987
NC_012920.1(MT-ND1):m.4160T>C	rs199476119
m.3376G>A	rs397515612
m.3700G>A	rs397515508
m.3733G>A	rs199476125
m.4171C>A	rs28616230

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