RS778854412 PLEKHG5

Health Risk Chr 1:6468048
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Associated Conditions
Inborn genetic diseases
Neuronopathy
distal hereditary motor
autosomal recessive 4
Charcot-Marie-Tooth disease recessive intermediate C
Inborn genetic diseases
Neuronopathy
distal hereditary motor
autosomal recessive 4
Charcot-Marie-Tooth disease recessive intermediate C
Other Variants in PLEKHG5
rs63750315 rs397515454 rs397515455 rs373184968 rs150807400 rs199794578 rs202191898 rs140202670 rs141032388 rs112530241
Ask Dr. Hemsworth about this variant