RS770272088 HSPB1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Charcot-Marie-Tooth disease axonal type 2F
Charcot-Marie-Tooth disease
Inborn genetic diseases
Distal hereditary motor neuropathy type 2
Neuronopathy
distal hereditary motor
type 2B
Distal spinal muscular atrophy
Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease axonal type 2F
HSPB1-related disorder
Neuronopathy
distal hereditary motor
type 2B
Charcot-Marie-Tooth disease axonal type 2F
Other Variants in HSPB1