RS587777712 ARHGEF10

Health Risk Chr 8:1882687
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What This Variant Does
"CLNSIG=4
Associated Conditions
Charcot-Marie-Tooth disease
Autosomal dominant slowed nerve conduction velocity
Charcot-Marie-Tooth disease
Autosomal dominant slowed nerve conduction velocity
Other Variants in ARHGEF10
rs147531758 rs143290224 rs1057523214 rs756594069 rs145754440 rs148715187 rs151080025 rs35925274 rs150226594 rs34036746
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