RS863224974 GJB1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Charcot-Marie-Tooth Neuropathy X
Inborn genetic diseases
Charcot-Marie-Tooth disease X-linked dominant 1
Charcot-Marie-Tooth disease X-linked dominant 1
Charcot-Marie-Tooth Neuropathy X
Inborn genetic diseases
Charcot-Marie-Tooth disease X-linked dominant 1
Charcot-Marie-Tooth disease X-linked dominant 1
Other Variants in GJB1