RS281865061 PRX
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What This Variant Does
"CLNSIG=5
Associated Conditions
Charcot-Marie-Tooth disease type 4F
Dejerine-Sottas disease
Autosomal recessive Dejerine-Sottas syndrome
Charcot-Marie-Tooth disease type 4F
Dejerine-Sottas disease
Autosomal recessive Dejerine-Sottas syndrome
Other Variants in PRX