ClinVar Miner

List of variants reported as likely pathogenic for Leigh syndrome by Mitochondrial Research Group, Murdoch Children's Research Institute

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_017446.4(MRPL39):c.589-924G>A	rs1209423257	0.00005
NM_017446.4(MRPL39):c.921+5G>A	rs375392547	0.00001

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