RS104894161 EGR2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Dejerine-sottas neuropathy
autosomal dominant
Charcot-Marie-Tooth disease type 1D
Dejerine-Sottas disease
Charcot-Marie-Tooth disease
type I
Charcot-Marie-Tooth disease
type I
Charcot-Marie-Tooth disease type 1D
Dejerine-sottas neuropathy
autosomal dominant
Charcot-Marie-Tooth disease type 1D
Dejerine-Sottas disease
Charcot-Marie-Tooth disease
type I
Other Variants in EGR2