List of variants in gene MT-CYB 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: 36

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.14750A>T	rs1603224853
NC_012920.1(MT-CYB):m.14832C>T	rs1603224915
NC_012920.1(MT-CYB):m.14841A>G	rs1556424497
NC_012920.1(MT-CYB):m.14871T>C	rs28660155
NC_012920.1(MT-CYB):m.14879A>T	rs1603224945
NC_012920.1(MT-CYB):m.14954A>G	rs1603224977
NC_012920.1(MT-CYB):m.14996G>A	rs1603225010
NC_012920.1(MT-CYB):m.15024G>C	rs1603225028
NC_012920.1(MT-CYB):m.15090T>C	rs1603225069
NC_012920.1(MT-CYB):m.15099T>C	rs1603225077
NC_012920.1(MT-CYB):m.15122A>G	rs1556424535
NC_012920.1(MT-CYB):m.15212A>G	rs1603225150
NC_012920.1(MT-CYB):m.15213T>C	rs1603225151
NC_012920.1(MT-CYB):m.15312T>C	rs1603225215
NC_012920.1(MT-CYB):m.15377A>G	rs1603225248
NC_012920.1(MT-CYB):m.15380A>G	rs1603225250
NC_012920.1(MT-CYB):m.15381C>T	rs199721378
NC_012920.1(MT-CYB):m.15434C>T	rs1603225279
NC_012920.1(MT-CYB):m.15450T>C	rs1603225291
NC_012920.1(MT-CYB):m.15467A>G	rs1569484723
NC_012920.1(MT-CYB):m.15521G>A	rs1603225327
NC_012920.1(MT-CYB):m.15533A>G	rs1556424601
NC_012920.1(MT-CYB):m.15650G>A	rs1556424635
NC_012920.1(MT-CYB):m.15654T>C	rs1556424638
NC_012920.1(MT-CYB):m.15657T>C	rs1556424640
NC_012920.1(MT-CYB):m.15664C>A	rs1603225414
NC_012920.1(MT-CYB):m.15732C>T	rs879129589
NC_012920.1(MT-CYB):m.15774T>C	rs1603225473
NC_012920.1(MT-CYB):m.15776A>G	rs1603225477
NC_012920.1(MT-CYB):m.15779T>C	rs1603225480
NC_012920.1(MT-CYB):m.15791A>G	rs1556424666
NC_012920.1(MT-CYB):m.15813T>G	rs1603225521
NC_012920.1(MT-CYB):m.15828C>T	rs1603225527
NC_012920.1(MT-CYB):m.15860A>T	rs201023973
NC_012920.1:m.15098A>G	rs527236172
NC_012920.1:m.15459C>T	rs527236186

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