rs387906709, UBQLN2

N. diseases: 9
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
AMYOTROPHIC LATERAL SCLEROSIS 15, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA
9 0.776 0.120 X 56565363 missense variant C/A;T snv 0.800 1.000 6 2011 2015
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.776 0.120 X 56565363 missense variant C/A;T snv 0.020 1.000 2 2014 2015
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.776 0.120 X 56565363 missense variant C/A;T snv 0.020 1.000 2 2019 2019
Amyotrophic Lateral Sclerosis, Familial
68 0.776 0.120 X 56565363 missense variant C/A;T snv 0.010 1.000 1 2019 2019
Cognition Disorders
CUI: C0009241
Disease: Cognition Disorders
47 0.776 0.120 X 56565363 missense variant C/A;T snv 0.010 1.000 1 2015 2015
Dementia
CUI: C0497327
Disease: Dementia
176 0.776 0.120 X 56565363 missense variant C/A;T snv 0.010 1.000 1 2014 2014
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.776 0.120 X 56565363 missense variant C/A;T snv 0.010 1.000 1 2015 2015
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.776 0.120 X 56565363 missense variant C/A;T snv 0.010 1.000 1 2019 2019
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.776 0.120 X 56565363 missense variant C/A;T snv 0.010 1.000 1 2014 2014