List of variants in gene MT-ND1 reported as uncertain significance 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: 54

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND1):m.3307A>T	rs1603218882
NC_012920.1(MT-ND1):m.3308delinsAC	rs1603218887
NC_012920.1(MT-ND1):m.3310C>T	rs1603218889
NC_012920.1(MT-ND1):m.3313A>G	rs1603218891
NC_012920.1(MT-ND1):m.3316G>C	rs2853516
NC_012920.1(MT-ND1):m.3320A>G	rs1603218896
NC_012920.1(MT-ND1):m.3328C>T	rs1603218901
NC_012920.1(MT-ND1):m.3357G>C	rs1556422714
NC_012920.1(MT-ND1):m.3358G>A	rs1556422715
NC_012920.1(MT-ND1):m.3395A>C	rs1556422722
NC_012920.1(MT-ND1):m.3419A>G	rs1603218949
NC_012920.1(MT-ND1):m.3427G>A	rs1603218960
NC_012920.1(MT-ND1):m.3488T>C	rs1603218982
NC_012920.1(MT-ND1):m.3496G>A	rs1603218984
NC_012920.1(MT-ND1):m.3508A>G	rs1603218990
NC_012920.1(MT-ND1):m.3509T>C	rs1603218992
NC_012920.1(MT-ND1):m.3526G>A	rs1603218998
NC_012920.1(MT-ND1):m.3569C>T	rs1603219022
NC_012920.1(MT-ND1):m.3607G>A	rs1556422761
NC_012920.1(MT-ND1):m.3622C>A	rs1603219048
NC_012920.1(MT-ND1):m.3643G>A	rs1603219061
NC_012920.1(MT-ND1):m.3652A>G	rs1603219066
NC_012920.1(MT-ND1):m.3653T>C	rs1603219067
NC_012920.1(MT-ND1):m.3661T>G	rs1603219070
NC_012920.1(MT-ND1):m.3670G>A	rs1603219074
NC_012920.1(MT-ND1):m.3701C>T	rs1603219086
NC_012920.1(MT-ND1):m.3709G>A	rs1603219090
NC_012920.1(MT-ND1):m.3710C>T	rs1603219093
NC_012920.1(MT-ND1):m.3712G>A	rs1603219095
NC_012920.1(MT-ND1):m.3713T>C	rs1603219096
NC_012920.1(MT-ND1):m.3715G>A	rs1603219097
NC_012920.1(MT-ND1):m.3749T>C	rs1603219116
NC_012920.1(MT-ND1):m.3751A>G	rs1603219119
NC_012920.1(MT-ND1):m.3764C>T	rs1603219127
NC_012920.1(MT-ND1):m.3772A>G	rs1603219135
NC_012920.1(MT-ND1):m.3775A>T	rs1603219137
NC_012920.1(MT-ND1):m.3793T>C	rs1603219148
NC_012920.1(MT-ND1):m.3887A>G	rs1603219185
NC_012920.1(MT-ND1):m.3910G>A	rs1603219195
NC_012920.1(MT-ND1):m.3928G>C	rs587776442
NC_012920.1(MT-ND1):m.3937T>C	rs1603219204
NC_012920.1(MT-ND1):m.4055T>C	rs1603219279
NC_012920.1(MT-ND1):m.4082T>C	rs1603219291
NC_012920.1(MT-ND1):m.4094C>T	rs1603219299
NC_012920.1(MT-ND1):m.4105A>G	rs1603219306
NC_012920.1(MT-ND1):m.4148G>A	rs1603219323
NC_012920.1(MT-ND1):m.4153G>A	rs28566134
NC_012920.1(MT-ND1):m.4165C>G	rs1603219331
NC_012920.1(MT-ND1):m.4180A>G	rs1603219342
NC_012920.1(MT-ND1):m.4193T>C	rs1603219346
NC_012920.1(MT-ND1):m.4211T>C	rs1603219356
NC_012920.1(MT-ND1):m.4238T>C	rs1603219369
NC_012920.1(MT-ND1):m.4247T>C	rs1603219376
NC_012920.1(MT-ND1):m.4258A>G	rs1603219383

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