List of variants in gene MT-ND4 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: 38

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND4):m.10845C>T	rs1603222985
NC_012920.1(MT-ND4):m.10895A>G	rs1603223008
NC_012920.1(MT-ND4):m.10899A>G	rs1603223010
NC_012920.1(MT-ND4):m.10907T>C	rs879094052
NC_012920.1(MT-ND4):m.10914G>A	rs878931758
NC_012920.1(MT-ND4):m.10920C>T	rs1556423876
NC_012920.1(MT-ND4):m.11016G>A	rs28594904
NC_012920.1(MT-ND4):m.11025T>C	rs201300253
NC_012920.1(MT-ND4):m.11061C>T	rs879204439
NC_012920.1(MT-ND4):m.11087T>C	rs28433448
NC_012920.1(MT-ND4):m.11150G>A	rs386829118
NC_012920.1(MT-ND4):m.11151C>T	rs1556423903
NC_012920.1(MT-ND4):m.11172A>G	rs2853489
NC_012920.1(MT-ND4):m.11177C>T	rs28358284
NC_012920.1(MT-ND4):m.11204T>C	rs201803443
NC_012920.1(MT-ND4):m.11252A>G	rs879229170
NC_012920.1(MT-ND4):m.11255T>C	rs1556423916
NC_012920.1(MT-ND4):m.11337A>G	rs1603223247
NC_012920.1(MT-ND4):m.11361T>C	rs1603223259
NC_012920.1(MT-ND4):m.11447G>A	rs2853492
NC_012920.1(MT-ND4):m.11654A>G	rs1603223374
NC_012920.1(MT-ND4):m.11928A>G	rs1569484466
NC_012920.1(MT-ND4):m.11963G>A	rs201803948
NC_012920.1(MT-ND4):m.11969G>A	rs28359169
NC_012920.1(MT-ND4):m.12020C>T	rs1603223516
NC_012920.1(MT-ND4):m.12026A>G	rs202136725
NC_012920.1(MT-ND4):m.12030A>G	rs1556424041
NC_012920.1(MT-ND4):m.12063C>T	rs1603223527
NC_012920.1(MT-ND4):m.12083T>G	rs1556424049
NC_012920.1(MT-ND4):m.12084C>T	rs1556424051
NC_012920.1(MT-ND4):m.12092C>A	rs1603223542
NC_012920.1(MT-ND4):m.12092C>T	rs1603223542
NC_012920.1(MT-ND4):m.12123C>T	rs1569484488
NC_012920.1(MT-ND4):m.12135C>A	rs1556424062
NC_012920.1:m.11984T>C	rs200911567
m.11084A>G	rs199476113
m.11253T>C	rs200145866
m.11696G>A	rs200873900

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