List of variants in gene MT-ND5 reported as pathogenic

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: 15

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND5):m.12425del	rs1603223730
NC_012920.1(MT-ND5):m.13063G>A	rs1603224017
NC_012920.1:m.13051G>A	rs1131692063
NC_012920.1:m.13094T>C	rs1603224029
NC_012920.1:m.13514A>G	rs587776440
m.12338T>C	rs201863060
m.12706T>C	rs267606893
m.12770A>G	rs267606894
m.12848C>T	rs267606899
m.13042G>A	rs267606898
m.13045A>C	rs267606895
m.13084A>T	rs267606896
m.13513G>A	rs267606897
m.13708G>A	rs28359178
m.13730G>A	rs387906425

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