Source: ALL

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: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.030 1.000 3 2013 2017
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.030 1.000 3 2013 2017
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.030 1.000 3 2013 2017
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.020 1.000 2 2008 2010
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.020 1.000 2 2015 2016
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.020 1.000 2 2015 2016
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.010 1.000 1 2018 2018
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C1277187
Disease: Left ventricular systolic dysfunction
Left ventricular systolic dysfunction 		0.010 1.000 1 2012 2012
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.010 1.000 1 2018 2018
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0018801
Disease: Heart failure
Heart failure 		0.010 1.000 1 2012 2012
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		0.010 1.000 1 2018 2018
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.010 1.000 1 2019 2019
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.010 1.000 1 2019 2019
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0342257
Disease: Complications of Diabetes Mellitus
Complications of Diabetes Mellitus 		0.010 1.000 1 2019 2019
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2014 2014
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2019 2019
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		0.010 1.000 1 2017 2017
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
Secondary malignant neoplasm of lymph node 		0.010 1.000 1 2018 2018
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 1.000 1 2018 2018
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.010 1.000 1 2018 2018
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 < 0.001 1 2015 2015
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.010 1.000 1 2012 2012
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2013 2013