ClinVar Miner

List of variants reported as likely benign for Hereditary motor and sensory neuropathy with optic atrophy by Illumina Clinical Services Laboratory,Illumina

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Total variants: 11
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HGVS dbSNP
NM_014874.3(MFN2):c.-149-15T>G rs114306601
NM_014874.3(MFN2):c.1403G>A (p.Arg468His) rs138382758
NM_014874.3(MFN2):c.159C>T (p.Ser53=) rs61733200
NM_014874.3(MFN2):c.1818C>T (p.Gly606=) rs373843969
NM_014874.3(MFN2):c.2145C>T (p.Ala715=) rs571011689
NM_014874.3(MFN2):c.2146G>A (p.Ala716Thr) rs144860227
NM_014874.3(MFN2):c.408A>T (p.Val136=) rs78814413
NM_014874.3(MFN2):c.58C>T (p.His20Tyr) rs201715603
NM_014874.3(MFN2):c.892G>A (p.Gly298Arg) rs41278630
NM_014874.4(MFN2):c.205G>A (p.Val69Ile)
NM_014874.4(MFN2):c.2204+13C>T

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