List of variants in gene MT-ND2 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: 42

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND2):m.4500T>C	rs879007369
NC_012920.1(MT-ND2):m.4531C>T	rs1603219496
NC_012920.1(MT-ND2):m.4612T>C	rs1603219525
NC_012920.1(MT-ND2):m.4654C>T	rs1603219538
NC_012920.1(MT-ND2):m.4689A>G	rs1603219555
NC_012920.1(MT-ND2):m.4702A>G	rs1603219570
NC_012920.1(MT-ND2):m.4725A>C	rs1603219581
NC_012920.1(MT-ND2):m.4725A>T	rs1603219581
NC_012920.1(MT-ND2):m.4728A>G	rs1556422892
NC_012920.1(MT-ND2):m.4762T>C	rs1603219605
NC_012920.1(MT-ND2):m.4763C>A	rs1603219607
NC_012920.1(MT-ND2):m.4812G>A	rs1603219637
NC_012920.1(MT-ND2):m.4812G>C	rs1603219637
NC_012920.1(MT-ND2):m.4842A>G	rs1603219643
NC_012920.1(MT-ND2):m.4908C>T	rs1603219668
NC_012920.1(MT-ND2):m.4911T>G	rs1603219671
NC_012920.1(MT-ND2):m.4924G>C	rs386828956
NC_012920.1(MT-ND2):m.4944A>G	rs878971699
NC_012920.1(MT-ND2):m.5067A>G	rs1603219758
NC_012920.1(MT-ND2):m.5069A>T	rs1603219761
NC_012920.1(MT-ND2):m.5073A>G	rs1603219765
NC_012920.1(MT-ND2):m.5086C>T	rs1603219776
NC_012920.1(MT-ND2):m.5095T>C	rs1556422950
NC_012920.1(MT-ND2):m.5127A>G	rs1603219795
NC_012920.1(MT-ND2):m.5128A>G	rs1603219796
NC_012920.1(MT-ND2):m.5149C>T	rs1603219806
NC_012920.1(MT-ND2):m.5166A>G	rs1603219809
NC_012920.1(MT-ND2):m.5191C>T	rs1603219822
NC_012920.1(MT-ND2):m.5205T>C	rs1603219831
NC_012920.1(MT-ND2):m.5268A>G	rs1603219860
NC_012920.1(MT-ND2):m.5273A>T	rs1603219868
NC_012920.1(MT-ND2):m.5293G>A	rs28690990
NC_012920.1(MT-ND2):m.5295C>T	rs1556422970
NC_012920.1(MT-ND2):m.5298A>G	rs1603219886
NC_012920.1(MT-ND2):m.5316G>A	rs1603219895
NC_012920.1(MT-ND2):m.5319A>T	rs28456039
NC_012920.1(MT-ND2):m.5320C>T	rs1603219899
NC_012920.1(MT-ND2):m.5325A>T	rs1603219901
NC_012920.1(MT-ND2):m.5331C>G	rs200778062
NC_012920.1(MT-ND2):m.5452C>T	rs1556422991
NC_012920.1(MT-ND2):m.5484A>G	rs1603219979
NC_012920.1(MT-ND2):m.5494T>G	rs1556423001

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