rs1800764, None

N. diseases: 10
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.
Dementia
CUI: C0497327
Disease: Dementia
176 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 0.010 1.000 1 2017 2017
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 0.010 1.000 1 2014 2014
Neonatal Drug Withdrawal
CUI: C3540839
Disease: Neonatal Drug Withdrawal
3 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 0.010 1.000 1 2009 2009
Non-dipping
CUI: C1695689
Disease: Non-dipping
3 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 0.010 1.000 1 2014 2014
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 0.010 1.000 1 2017 2017
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 0.020 1.000 2 2007 2009
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 0.020 1.000 2 2013 2014
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 0.020 1.000 2 2014 2014
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 0.020 1.000 2 2005 2009
Mental deterioration
CUI: C0234985
Disease: Mental deterioration
121 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 0.020 1.000 2 2014 2014