List of variants in gene MT-CO3 reported as pathogenic for hereditary disease

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: 10

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CO3):m.9379G>A	rs267606615
NC_012920.1(MT-CO3):m.9438G>A	rs267606611
NC_012920.1(MT-CO3):m.9487_9501del	rs267606612
NC_012920.1(MT-CO3):m.9537dup	rs267606614
NC_012920.1(MT-CO3):m.9804G>A	rs200613617
NC_012920.1(MT-CO3):m.9952G>A	rs267606613
NC_012920.1:m.9237G>A	rs1057516064
NC_012920.1:m.9273_9274insATC	rs1569484288
NC_012920.1:m.9429_9430insCCC	rs1569484299
NC_012920.1:m.9441_9442insTTT	rs1569484301

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