RS29001571 HSPB1
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What This Variant Does
"[OMIM:NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB]
Associated Conditions
Neuronopathy
distal hereditary motor
type 2B
Charcot-Marie-Tooth disease axonal type 2F
Inborn genetic diseases
Neuronopathy
distal hereditary motor
type 2B
Charcot-Marie-Tooth disease axonal type 2F
Inborn genetic diseases
Other Variants in HSPB1