rs1800624, PBX2;AGER

N. diseases: 33
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.
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.020 1.000 2 2008 2010
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2010 2010
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2012 2012
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2012 2012
Left ventricular systolic dysfunction
CUI: C1277187
Disease: Left ventricular systolic dysfunction
11 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2012 2012
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.030 1.000 3 2013 2017
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.030 1.000 3 2013 2017
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.030 1.000 3 2013 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2013 2013
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2014 2014
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.020 1.000 2 2015 2016
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.020 1.000 2 2015 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1 2015 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1 2015 2015
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2017 2017
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2017 2017
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2017 2017
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2017 2017
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2017 2017
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2018 2018
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2018 2018
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2018 2018
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2018 2018
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.010 1.000 1 2018 2018