rs3825172, PSMD9

N. diseases: 14
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.
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 0.030 1.000 3 2011 2015
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 0.020 1.000 2 2014 2015
Carpal Tunnel Syndrome
CUI: C0007286
Disease: Carpal Tunnel Syndrome
46 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2014 2014
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2014 2014
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2014 2014
Generalized Anxiety Disorder
CUI: C0270549
Disease: Generalized Anxiety Disorder
24 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2014 2014
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2014 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2014 2014
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2014 2014
Mental Depression
CUI: C0011570
Disease: Mental Depression
271 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2014 2014
Neuropathy
CUI: C0442874
Disease: Neuropathy
110 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2014 2014
Obesity
CUI: C0028754
Disease: Obesity
1111 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2014 2014
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
56 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2014 2014
Sleeplessness
CUI: C0917801
Disease: Sleeplessness
30 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2015 2015