ClinVar Miner

List of variants studied for Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2A2B

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Total variants: 13
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NM_001127660.1(MFN2):c.154G>A (p.Glu52Lys) rs1553141017
NM_001127660.1(MFN2):c.526G>A (p.Gly176Ser) rs879253862
NM_014874.3(MFN2):c.1085C>T (p.Thr362Met) rs387906991
NM_014874.3(MFN2):c.2119C>T (p.Arg707Trp) rs119103267
NM_014874.3(MFN2):c.271G>T (p.Val91Leu) rs1557519001
NM_014874.3(MFN2):c.334G>A (p.Val112Met) rs757937208
NM_014874.3(MFN2):c.404G>A (p.Arg135Gln) rs1443036026
NM_014874.3(MFN2):c.491C>T (p.Ala164Val) rs1553142699
NM_014874.3(MFN2):c.647T>C (p.Phe216Ser) rs387906990
NM_014874.3(MFN2):c.842G>C (p.Cys281Ser) rs147136530
NM_014874.4(MFN2):c.107AGA[2] (p.Lys38del) rs1478175861
NM_014874.4(MFN2):c.1963A>G (p.Lys655Glu)

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