ClinVar Miner

List of variants reported as uncertain significance for Hereditary motor and sensory neuropathy with optic atrophy by Centre for Mendelian Genomics,University Medical Centre Ljubljana

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Total variants: 3
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NM_014874.3(MFN2):c.1858G>A (p.Val620Ile) rs200936779
NM_014874.3(MFN2):c.1946G>A (p.Arg649His) rs763492075
NM_014874.4(MFN2):c.1777T>A (p.Ser593Thr)

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