Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1265564
rs1265564
CUX2
1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.810 1.000 1 2012 2012
dbSNP: rs886126
rs886126
CUX2
1.000 0.040 12 111241410 intron variant C/T snv 0.34
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 1 2013 2013
dbSNP: rs79105258
rs79105258
CUX2
12 111280427 intron variant C/A;T snv
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 3 2018 2019
dbSNP: rs79105258
rs79105258
CUX2
12 111280427 intron variant C/A;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 2 2018 2018
dbSNP: rs79105258
rs79105258
CUX2
12 111280427 intron variant C/A;T snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 2 2018 2018
dbSNP: rs79105258
rs79105258
CUX2
12 111280427 intron variant C/A;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 2 2018 2018
dbSNP: rs79105258
rs79105258
CUX2
12 111280427 intron variant C/A;T snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 2 2018 2019
dbSNP: rs11830764
rs11830764
CUX2
12 111077216 intron variant G/A;C;T snv
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1265564
rs1265564
CUX2
1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2018 2018
dbSNP: rs1265564
rs1265564
CUX2
1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs1265564
rs1265564
CUX2
1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs147032946
rs147032946
CUX2
12 111151263 intron variant C/A;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs147032946
rs147032946
CUX2
12 111151263 intron variant C/A;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs2157999
rs2157999
CUX2
1.000 12 111266635 intron variant G/A snv 8.1E-02
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2019 2019
dbSNP: rs2157999
rs2157999
CUX2
1.000 12 111266635 intron variant G/A snv 8.1E-02
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2019 2019
dbSNP: rs2157999
rs2157999
CUX2
1.000 12 111266635 intron variant G/A snv 8.1E-02
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2019 2019
dbSNP: rs2157999
rs2157999
CUX2
1.000 12 111266635 intron variant G/A snv 8.1E-02
CUI: C0376705
Disease: Viral Load result
Viral Load result 		0.700 1.000 1 2019 2019
dbSNP: rs2157999
rs2157999
CUX2
1.000 12 111266635 intron variant G/A snv 8.1E-02
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2019 2019
dbSNP: rs2339717
rs2339717
CUX2
12 111258724 intron variant T/C snv 0.45
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs4766566
rs4766566
CUX2
0.851 0.200 12 111269073 intron variant C/T snv 0.42
CUI: C0018099
Disease: Gout
Gout 		0.700 1.000 1 2017 2017
dbSNP: rs4766566
rs4766566
CUX2
0.851 0.200 12 111269073 intron variant C/T snv 0.42
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs4766566
rs4766566
CUX2
0.851 0.200 12 111269073 intron variant C/T snv 0.42
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		0.700 1.000 1 2017 2017
dbSNP: rs4766566
rs4766566
CUX2
0.851 0.200 12 111269073 intron variant C/T snv 0.42
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2018 2018
dbSNP: rs6490061
rs6490061
CUX2
0.925 0.120 12 111335541 intron variant T/C snv 0.30
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 1.000 1 2018 2018
dbSNP: rs76721774
rs76721774
CUX2
12 111268872 intron variant A/C snv 1.1E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019