rs79105258, CUX2

N. diseases: 24
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.
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
1463 12 111280427 intron variant C/A;T snv 0.700 1.000 3 2018 2019
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 12 111280427 intron variant C/A;T snv 0.700 1.000 2 2018 2018
Glomerular Filtration Rate
CUI: C0017654
Disease: Glomerular Filtration Rate
1033 12 111280427 intron variant C/A;T snv 0.700 1.000 2 2018 2019
Mean blood pressure
CUI: C0428886
Disease: Mean blood pressure
344 12 111280427 intron variant C/A;T snv 0.700 1.000 2 2018 2018
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 12 111280427 intron variant C/A;T snv 0.700 1.000 2 2018 2018
Activated Partial Thromboplastin Time measurement
44 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Alanine aminotransferase measurement
77 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Aspartate aminotransferase measurement
76 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Blood urea nitrogen measurement
CUI: C0005845
Disease: Blood urea nitrogen measurement
174 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Chloride measurement
CUI: C0201952
Disease: Chloride measurement
19 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Corpuscular Hemoglobin Concentration Mean
4389 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Creatinine measurement, serum (procedure)
243 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
111 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Finding of Mean Corpuscular Hemoglobin
1206 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
111 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
High density lipoprotein measurement
1440 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Low density lipoprotein cholesterol measurement
1142 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Serum Alanine Aminotransferase Measurement
77 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Serum gamma-glutamyl transferase measurement
108 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Sodium measurement
CUI: C0337443
Disease: Sodium measurement
69 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Caffeine related disorders
CUI: C0236734
Disease: Caffeine related disorders
56 12 111280427 intron variant C/A;T snv 0.010 1.000 1 2019 2019