ClinVar Miner

List of variants studied for Leber hereditary optic neuropathy by GenomeConnect, ClinGen

Included ClinVar conditions (4):

Leber hereditary optic neuropathy with dystonia
Leber's optic atrophy
Leber's optic atrophy; Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
Leber's optic atrophy; Neuropathy ataxia retinitis pigmentosa syndrome; Mitochondrial DNA-Associated Leigh Syndrome and NARP

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Total variants: 2

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HGVS	dbSNP
NC_012920.1:m.11778G>A	rs199476112
NC_012920.1:m.8686T>C	rs1569484231

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