RS886039782 SQSTM1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neurodegeneration with ataxia
dystonia
and gaze palsy
childhood-onset
Paget disease of bone 2
early-onset
Frontotemporal dementia and/or amyotrophic lateral sclerosis 1
Neurodegeneration with ataxia
dystonia
and gaze palsy
childhood-onset
Paget disease of bone 2
early-onset
Frontotemporal dementia and/or amyotrophic lateral sclerosis 1
Other Variants in SQSTM1