RS1011669872 HSPB8
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Associated Conditions
Neuronopathy
distal hereditary motor
type 2A
Charcot-Marie-Tooth disease axonal type 2L
Inborn genetic diseases
Neuronopathy
distal hereditary motor
type 2A
Charcot-Marie-Tooth disease axonal type 2L
Inborn genetic diseases
Other Variants in HSPB8