RS797045102 PRX

Health Risk Chr 19:40396063
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal recessive Dejerine-Sottas syndrome
Charcot-Marie-Tooth disease type 4F
Charcot-Marie-Tooth disease type 4
Autosomal recessive Dejerine-Sottas syndrome
Charcot-Marie-Tooth disease type 4F
Charcot-Marie-Tooth disease type 4
Other Variants in PRX
rs104894714 rs104894715 rs104894706 rs104894707 rs104894708 rs281865061 rs147826200 rs147587689 rs200033507 rs754521978
Ask Dr. Hemsworth about this variant