RS775332895 CHCHD10
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What This Variant Does
"CLNSIG=5
Associated Conditions
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2
Autosomal dominant mitochondrial myopathy with exercise intolerance
Lower motor neuron syndrome with late-adult onset
Inborn genetic diseases
Amyotrophic lateral sclerosis
CHCHD10-related disorder
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2
Autosomal dominant mitochondrial myopathy with exercise intolerance
Lower motor neuron syndrome with late-adult onset
Inborn genetic diseases
Amyotrophic lateral sclerosis
CHCHD10-related disorder
Other Variants in CHCHD10