List of variants in gene MT-ATP6, MT-ATP8 studied 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
		ClinVar version:

Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NC_012920.1:m.8527A>G	rs878853003
NC_012920.1:m.8530A>G	rs1556423480
NC_012920.1:m.8531A>G	rs1556423481
NC_012920.1:m.8533G>A	rs386829039
NC_012920.1:m.8537A>G	rs1603221571
NC_012920.1:m.8540T>C	rs878852987
NC_012920.1:m.8541G>A	rs1569484218
NC_012920.1:m.8542T>C	rs1603221575
NC_012920.1:m.8545G>A	rs1603221578
NC_012920.1:m.8547T>C	rs1603221579
NC_012920.1:m.8548T>C	rs1603221580
NC_012920.1:m.8550A>G	rs1603221581
NC_012920.1:m.8551T>C	rs1556423486
NC_012920.1:m.8552T>C	rs1603221582
NC_012920.1:m.8553C>T	rs1569484219
NC_012920.1:m.8554A>G	rs1603221583
NC_012920.1:m.8557G>A	rs386829040
NC_012920.1:m.8557G>C	rs386829040
NC_012920.1:m.8562C>T	rs1603221584
NC_012920.1:m.8563A>G	rs386829041
NC_012920.1:m.8566A>G	rs3020563
NC_012920.1:m.8567T>C	rs1603221586
NC_012920.1:m.8568C>A	rs1603221589
NC_012920.1:m.8572G>A	rs28502681

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