List of variants in gene MT-ND6 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: 33

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND6):m.14162G>A	rs1603224571
NC_012920.1(MT-ND6):m.14163C>T	rs1603224574
NC_012920.1(MT-ND6):m.14178T>C	rs28357671
NC_012920.1(MT-ND6):m.14180T>C	rs200933339
NC_012920.1(MT-ND6):m.14198G>A	rs1603224596
NC_012920.1(MT-ND6):m.14207G>A	rs879217937
NC_012920.1(MT-ND6):m.14211C>T	rs1603224605
NC_012920.1(MT-ND6):m.14226G>A	rs1603224612
NC_012920.1(MT-ND6):m.14249G>A	rs1556424407
NC_012920.1(MT-ND6):m.14256T>C	rs1603224630
NC_012920.1(MT-ND6):m.14258G>A	rs202227543
NC_012920.1(MT-ND6):m.14259G>A	rs1603224632
NC_012920.1(MT-ND6):m.14280A>G	rs1603224649
NC_012920.1(MT-ND6):m.14312A>G	rs1603224665
NC_012920.1(MT-ND6):m.14315C>T	rs1603224668
NC_012920.1(MT-ND6):m.14318T>C	rs28357675
NC_012920.1(MT-ND6):m.14384G>A	rs1556424435
NC_012920.1(MT-ND6):m.14393A>G	rs878853104
NC_012920.1(MT-ND6):m.14405A>G	rs1603224713
NC_012920.1(MT-ND6):m.14417A>G	rs878905427
NC_012920.1(MT-ND6):m.14433C>T	rs1556424444
NC_012920.1(MT-ND6):m.14502T>C	rs201327354
NC_012920.1(MT-ND6):m.14514T>C	rs1603224772
NC_012920.1(MT-ND6):m.14552A>G	rs1556424459
NC_012920.1(MT-ND6):m.14553C>T	rs1603224787
NC_012920.1(MT-ND6):m.14562C>T	rs1603224791
NC_012920.1(MT-ND6):m.14571T>A	rs1603224793
NC_012920.1(MT-ND6):m.14574C>T	rs386829218
NC_012920.1(MT-ND6):m.14577T>C	rs386829219
NC_012920.1(MT-ND6):m.14582A>G	rs41354845
NC_012920.1(MT-ND6):m.14634T>C	rs1603224816
m.14319T>C	rs199476110
m.14325T>C	rs397515505

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