List of variants studied for Leigh syndrome by GeneReviews

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		ClinVar version:

Total variants: 37

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HGVS	dbSNP	gnomAD frequency
NC_012920.1:m.10254G>A	rs587776438
NC_012920.1:m.11984T>C	rs200911567
NC_012920.1:m.13514A>G	rs587776440
NC_012920.1:m.14484T>C	rs199476104
NC_012920.1:m.1644G>T	rs587776441
NC_012920.1:m.3243A>G	rs199474657
NC_012920.1:m.3460G>A	rs199476118
NC_012920.1:m.3481G>A	rs587776433
NC_012920.1:m.3890G>A	rs587776434
NC_012920.1:m.3928G>C	rs587776442
NC_012920.1:m.5523T>G	rs587776435
NC_012920.1:m.5559A>G	rs1556423008
NC_012920.1:m.8839G>C	rs1556423547
NC_012920.1:m.8851T>C	rs199476136
NC_012920.1:m.8989G>C	rs587776444
NC_012920.1:m.8993T>C	rs199476133
NC_012920.1:m.8993T>G	rs199476133
NC_012920.1:m.9176T>C	rs199476135
NC_012920.1:m.9176T>G	rs199476135
NC_012920.1:m.9185T>C	rs199476138
NC_012920.1:m.9191T>C	rs1556423632
NC_012920.1:m.9478T>C	rs587776437
m.10158T>C	rs199476117
m.10191T>C	rs267606890
m.10197G>A	rs267606891
m.11777C>A	rs28384199
m.12706T>C	rs267606893
m.13513G>A	rs267606897
m.14459G>A	rs199476105
m.14487T>C	rs199476109
m.1624C>T	rs199476144
m.4681T>C	rs267606889
m.5537_5538insT	rs199474672
m.8344A>G	rs118192098
m.8363G>A	rs118192100
m.9537dupC	rs267606614
mitochondrial DNA deletion

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