RS200396166 SQSTM1

Health Risk Chr 5:179821034
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What This Variant Does
"CLNSIG=5
Associated Conditions
Frontotemporal dementia and/or amyotrophic lateral sclerosis 3
Frontotemporal dementia and/or amyotrophic lateral sclerosis 1
Paget disease of bone 2
early-onset
Paget disease of bone 3
Inborn genetic diseases
Cervical cancer
Frontotemporal dementia and/or amyotrophic lateral sclerosis 3
Frontotemporal dementia and/or amyotrophic lateral sclerosis 1
Paget disease of bone 2
early-onset
Paget disease of bone 3
Inborn genetic diseases
Cervical cancer
Other Variants in SQSTM1
rs104893941 rs796051869 rs796051870 rs796052213 rs776749939 rs139482113 rs886039780 rs886039781 rs886039782 rs370970067
Ask Dr. Hemsworth about this variant