RS202191898 PLEKHG5

Health Risk Chr 1:6468378
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What This Variant Does
"CLNSIG=5
Associated Conditions
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
Inborn genetic diseases
Other Variants in PLEKHG5
rs63750315 rs397515454 rs397515455 rs373184968 rs150807400 rs199794578 rs140202670 rs141032388 rs112530241 rs886042289
Ask Dr. Hemsworth about this variant