rs1728918, None

N. diseases: 19
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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.800 1.000 1 2012 2012
Body mass index
CUI: C1305855
Disease: Body mass index
2689 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 2 2016 2019
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016
Creatinine measurement, serum (procedure)
243 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2019 2019
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
111 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
111 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016
High density lipoprotein measurement
1440 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2012 2012
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 0.700 1.000 1 2016 2016