ClinVar Miner

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

Included ClinVar conditions (7):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ATP6):m.8686T>C	rs1569484231
NC_012920.1(MT-CYB):m.15485C>T	rs2520750122
NC_012920.1(MT-ND4):m.11778G>A	rs199476112
NC_012920.1(MT-ND5):m.13763C>T	rs1603224344
NC_012920.1(MT-ND6):m.14484T>C	rs199476104

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