List of variants in gene MT-CO2 reported as likely 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: 18

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CO2):m.7637G>A	rs1556423314
NC_012920.1(MT-CO2):m.7649A>G	rs1603221060
NC_012920.1(MT-CO2):m.7674T>C	rs1569484168
NC_012920.1(MT-CO2):m.7761A>G	rs1603221122
NC_012920.1(MT-CO2):m.7772A>G	rs1603221127
NC_012920.1(MT-CO2):m.7784A>G	rs1556423348
NC_012920.1(MT-CO2):m.7785T>C	rs1603221138
NC_012920.1(MT-CO2):m.7796A>G	rs1603221141
NC_012920.1(MT-CO2):m.7797T>C	rs1603221143
NC_012920.1(MT-CO2):m.7808C>T	rs1603221148
NC_012920.1(MT-CO2):m.7941A>G	rs1603221223
NC_012920.1(MT-CO2):m.8021A>G	rs1603221261
NC_012920.1(MT-CO2):m.8075G>A	rs386829024
NC_012920.1(MT-CO2):m.8078G>A	rs878993263
NC_012920.1(MT-CO2):m.8084A>G	rs1057518824
NC_012920.1(MT-CO2):m.8084A>T	rs1057518824
NC_012920.1(MT-CO2):m.8256T>C	rs1603221354
NC_012920.1(MT-CO2):m.8258T>C	rs1603221357

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