List of variants in gene MT-ND1 reported as uncertain significance by Stanford Center for Inherited Cardiovascular Disease, Stanford University

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:m.3548T>C	rs876661353
NC_012920.1:m.3907G>A	rs876661354
NC_012920.1:m.3918G>C	rs28357972
NC_012920.1:m.4135T>C	rs876661355

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