List of variants in gene MT-CO2 reported as benign for Leigh syndrome

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: 25

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CO2):m.7598G>A	rs386420012
NC_012920.1(MT-CO2):m.7604G>A	rs1603221034
NC_012920.1(MT-CO2):m.7664G>A	rs879139393
NC_012920.1(MT-CO2):m.7673A>G	rs1569484167
NC_012920.1(MT-CO2):m.7679T>C	rs879003775
NC_012920.1(MT-CO2):m.7691T>C	rs1603221084
NC_012920.1(MT-CO2):m.7697G>A	rs879212765
NC_012920.1(MT-CO2):m.7724A>T	rs1553139599
NC_012920.1(MT-CO2):m.7746A>G	rs1603221113
NC_012920.1(MT-CO2):m.7754G>A	rs1556423339
NC_012920.1(MT-CO2):m.7757G>A	rs1603221120
NC_012920.1(MT-CO2):m.7775G>A	rs1556423347
NC_012920.1(MT-CO2):m.7805G>A	rs879119797
NC_012920.1(MT-CO2):m.7830G>A	rs878897170
NC_012920.1(MT-CO2):m.7844A>G	rs1556423353
NC_012920.1(MT-CO2):m.7853G>A	rs386420037
NC_012920.1(MT-CO2):m.7854T>C	rs1603221180
NC_012920.1(MT-CO2):m.7859G>A	rs373105186
NC_012920.1(MT-CO2):m.7934A>G	rs374261450
NC_012920.1(MT-CO2):m.7964T>C	rs1556423367
NC_012920.1(MT-CO2):m.8022T>C	rs1556423376
NC_012920.1(MT-CO2):m.8026A>T	rs1603221263
NC_012920.1(MT-CO2):m.8027G>A	rs1116904
NC_012920.1(MT-CO2):m.8108A>G	rs1603221288
NC_012920.1(MT-CO2):m.8237A>G	rs1603221342

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