ClinVar Miner

List of variants reported as uncertain significance for Amyotrophic lateral sclerosis type 5; Spastic paraplegia 11, autosomal recessive; Charcot-Marie-Tooth disease, axonal type 2X

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Total variants: 5
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NM_025137.4(SPG11):c.3425C>G (p.Ser1142Cys) rs201082396
NM_025137.4(SPG11):c.5471G>A (p.Arg1824Gln) rs752401008
NM_025137.4(SPG11):c.6043G>A (p.Asp2015Asn) rs771242219
NM_025137.4(SPG11):c.604A>G (p.Met202Val) rs201875705
NM_025137.4(SPG11):c.6625C>T (p.Arg2209Cys) rs374057859

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