RS137930278 BSCL2
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Associated Conditions
Charcot-Marie-Tooth disease type 2
Inborn genetic diseases
Hereditary spastic paraplegia 17
Neuronopathy
distal hereditary motor
type 5C
Congenital generalized lipodystrophy type 2
Severe neurodegenerative syndrome with lipodystrophy
Charcot-Marie-Tooth disease type 2
Inborn genetic diseases
Hereditary spastic paraplegia 17
Neuronopathy
distal hereditary motor
type 5C
Congenital generalized lipodystrophy type 2
Other Variants in BSCL2