RS771657338 SQSTM1

Health Risk Chr 5:179836477
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Associated Conditions
Frontotemporal dementia and/or amyotrophic lateral sclerosis 1
Paget disease of bone 2
early-onset
Inborn genetic diseases
Frontotemporal dementia and/or amyotrophic lateral sclerosis 1
Paget disease of bone 2
early-onset
Inborn genetic diseases
Other Variants in SQSTM1
rs104893941 rs796051869 rs796051870 rs796052213 rs776749939 rs200396166 rs139482113 rs886039780 rs886039781 rs886039782
Ask Dr. Hemsworth about this variant