RS587777882 NEFL
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What This Variant Does
"CLNSIG=4
Associated Conditions
Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease type 2E
Inborn genetic diseases
Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease type 2E
Inborn genetic diseases
Other Variants in NEFL