List of variants in gene MT-ATP6 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: 47

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ATP6):m.8596A>G	rs1603221617
NC_012920.1(MT-ATP6):m.8597T>C	rs1603221620
NC_012920.1(MT-ATP6):m.8617A>G	rs1603221641
NC_012920.1(MT-ATP6):m.8623A>G	rs1603221645
NC_012920.1(MT-ATP6):m.8624C>T	rs1603221647
NC_012920.1(MT-ATP6):m.8626T>C	rs1603221648
NC_012920.1(MT-ATP6):m.8635C>T	rs1603221661
NC_012920.1(MT-ATP6):m.8638A>G	rs1556423508
NC_012920.1(MT-ATP6):m.8648G>A	rs28479867
NC_012920.1(MT-ATP6):m.8656A>G	rs1603221673
NC_012920.1(MT-ATP6):m.8657C>T	rs1603221675
NC_012920.1(MT-ATP6):m.8666A>G	rs1603221681
NC_012920.1(MT-ATP6):m.8679A>C	rs386829045
NC_012920.1(MT-ATP6):m.8704A>G	rs878852994
NC_012920.1(MT-ATP6):m.8711A>G	rs1556423524
NC_012920.1(MT-ATP6):m.8713A>G	rs1603221721
NC_012920.1(MT-ATP6):m.8750T>C	rs1603221765
NC_012920.1(MT-ATP6):m.8765C>T	rs1603221781
NC_012920.1(MT-ATP6):m.8767A>G	rs1603221783
NC_012920.1(MT-ATP6):m.8803A>G	rs878853020
NC_012920.1(MT-ATP6):m.8842A>C	rs386829052
NC_012920.1(MT-ATP6):m.8888T>C	rs1603221880
NC_012920.1(MT-ATP6):m.8895T>A	rs1603221884
NC_012920.1(MT-ATP6):m.8908T>C	rs1603221898
NC_012920.1(MT-ATP6):m.8923A>G	rs200329150
NC_012920.1(MT-ATP6):m.8930C>T	rs1603221915
NC_012920.1(MT-ATP6):m.8939T>C	rs1603221925
NC_012920.1(MT-ATP6):m.8944A>G	rs1603221929
NC_012920.1(MT-ATP6):m.8966T>C	rs1556423580
NC_012920.1(MT-ATP6):m.8974C>G	rs1603221949
NC_012920.1(MT-ATP6):m.8975T>C	rs1981459
NC_012920.1(MT-ATP6):m.8981A>G	rs1603221955
NC_012920.1(MT-ATP6):m.8986A>G	rs1603221956
NC_012920.1(MT-ATP6):m.8987T>C	rs1603221957
NC_012920.1(MT-ATP6):m.8989G>A	rs587776444
NC_012920.1(MT-ATP6):m.8999T>C	rs1603221963
NC_012920.1(MT-ATP6):m.9007A>T	rs1603221973
NC_012920.1(MT-ATP6):m.9010G>A	rs1556423589
NC_012920.1(MT-ATP6):m.9016A>G	rs1556423591
NC_012920.1(MT-ATP6):m.9038T>C	rs1603222003
NC_012920.1(MT-ATP6):m.9071C>T	rs1603222032
NC_012920.1(MT-ATP6):m.9079A>G	rs1603222038
NC_012920.1(MT-ATP6):m.9091A>G	rs1057520079
NC_012920.1(MT-ATP6):m.9095T>C	rs1603222056
NC_012920.1(MT-ATP6):m.9130C>A	rs1603222113
NC_012920.1:m.9152T>C	rs878853096
NC_012920.1:m.9157G>A	rs1556423625

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