List of variants in gene MT-ND6 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: 16

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND6):m.14153T>C	rs1603224565
NC_012920.1(MT-ND6):m.14181A>G	rs1603224581
NC_012920.1(MT-ND6):m.14189A>G	rs1603224589
NC_012920.1(MT-ND6):m.14193A>G	rs1556424397
NC_012920.1(MT-ND6):m.14280A>C	rs1603224649
NC_012920.1(MT-ND6):m.14334C>T	rs1603224679
NC_012920.1(MT-ND6):m.14340C>T	rs1603224683
NC_012920.1(MT-ND6):m.14348T>C	rs1603224685
NC_012920.1(MT-ND6):m.14357A>G	rs1603224692
NC_012920.1(MT-ND6):m.14420C>T	rs1556424442
NC_012920.1(MT-ND6):m.14462G>A	rs1603224737
NC_012920.1(MT-ND6):m.14529C>T	rs1603224782
NC_012920.1(MT-ND6):m.14564A>G	rs1556424461
NC_012920.1(MT-ND6):m.14577T>G	rs386829219
NC_012920.1(MT-ND6):m.14633A>G	rs1569484667
NC_012920.1:m.14598T>C	rs1057518882

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