RS1057518943 IGHMBP2
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What This Variant Does
"CLNSIG=4
Associated Conditions
Lower limb muscle weakness
Difficulty walking
Inability to walk
Hammertoe
Progressive muscle weakness
Autosomal recessive distal spinal muscular atrophy 1
Charcot-Marie-Tooth disease axonal type 2S
Charcot-Marie-Tooth disease axonal type 2S
Autosomal recessive distal spinal muscular atrophy 1
Inborn genetic diseases
Lower limb muscle weakness
Difficulty walking
Inability to walk
Hammertoe
Progressive muscle weakness
Other Variants in IGHMBP2