List of variants reported as not provided for Leigh syndrome by GeneReviews

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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-ATP6):m.8839G>C	rs1556423547
NC_012920.1(MT-ATP6):m.8851T>C	rs199476136
NC_012920.1(MT-ATP6):m.8989G>C	rs587776444
NC_012920.1(MT-ATP6):m.8993T>C	rs199476133
NC_012920.1(MT-ATP6):m.8993T>G	rs199476133
NC_012920.1(MT-ATP6):m.9176T>C	rs199476135
NC_012920.1(MT-ATP6):m.9176T>G	rs199476135
NC_012920.1(MT-ATP6):m.9185T>C	rs199476138
NC_012920.1(MT-ATP6):m.9191T>C	rs1556423632
NC_012920.1(MT-CO3):m.9478T>C	rs587776437
NC_012920.1(MT-CO3):m.9537dup	rs267606614
NC_012920.1(MT-ND1):m.1624C>T	rs199476144
NC_012920.1(MT-ND1):m.1644G>T	rs587776441
NC_012920.1(MT-ND1):m.3460G>A	rs199476118
NC_012920.1(MT-ND1):m.3481G>A	rs587776433
NC_012920.1(MT-ND1):m.3890G>A	rs587776434
NC_012920.1(MT-ND1):m.3928G>C	rs587776442
NC_012920.1(MT-ND2):m.4681T>C	rs267606889
NC_012920.1(MT-ND3):m.10158T>C	rs199476117
NC_012920.1(MT-ND3):m.10191T>C	rs267606890
NC_012920.1(MT-ND3):m.10197G>A	rs267606891
NC_012920.1(MT-ND3):m.10254G>A	rs587776438
NC_012920.1(MT-ND4):m.11777C>A	rs28384199
NC_012920.1(MT-ND4):m.11984T>C	rs200911567
NC_012920.1(MT-ND5):m.12706T>C (p.Phe124Leu)	rs267606893
NC_012920.1(MT-ND5):m.13513G>A	rs267606897
NC_012920.1(MT-ND5):m.13514A>G	rs587776440
NC_012920.1(MT-ND6):m.14459G>A	rs199476105
NC_012920.1(MT-ND6):m.14484T>C	rs199476104
NC_012920.1(MT-ND6):m.14487T>C	rs199476109
NC_012920.1(MT-TK):m.8344A>G	rs118192098
NC_012920.1(MT-TK):m.8363G>A	rs118192100
NC_012920.1(MT-TL1):m.3243A>G	rs199474657
NC_012920.1(MT-TW):m.5523T>G	rs587776435
NC_012920.1(MT-TW):m.5537_5538insT	rs199474672
NC_012920.1(MT-TW):m.5559A>G	rs1556423008

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