ClinVar Miner

List of variants reported as uncertain significance for Mitochondrial disease by Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.15192T>G
NC_012920.1(MT-ND5):m.13345G>A

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