ClinVar Miner

List of variants in gene MT-ND5 reported as pathogenic for Leigh syndrome

Included ClinVar conditions (11):

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: 3

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND5):m.13112T>C	rs1603224043
NC_012920.1(MT-ND5):m.13513G>A	rs267606897
NC_012920.1(MT-ND5):m.13514A>G	rs587776440

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