rs4646903, CYP1A1

N. diseases: 36
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.
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.050 1.000 5 2011 2017
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.050 1.000 5 2011 2017
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.050 1.000 5 2011 2017
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.040 0.750 4 2010 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.040 0.750 4 2016 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.040 1.000 4 2010 2017
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.040 0.750 4 2010 2016
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.040 0.750 4 2010 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.020 1.000 2 2007 2007
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.020 1.000 2 2014 2019
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.020 1.000 2 2014 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.020 1.000 2 2007 2007
Malignant neoplasm of colon and/or rectum
502 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.020 1.000 2 2016 2017
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.020 1.000 2 2014 2019
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.020 1.000 2 2013 2014
Acute respiratory failure
CUI: C0264490
Disease: Acute respiratory failure
5 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.010 1.000 1 2013 2013
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.010 1.000 1 2013 2013
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.010 1.000 1 2014 2014
Carcinoma of larynx
CUI: C0595989
Disease: Carcinoma of larynx
65 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.010 1.000 1 2016 2016
Chronic stable plaque psoriasis
CUI: C1304119
Disease: Chronic stable plaque psoriasis
4 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.010 1.000 1 2016 2016
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.010 1.000 1 2010 2010
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.010 1.000 1 2010 2010
Gastric Cardia Carcinoma
CUI: C1333763
Disease: Gastric Cardia Carcinoma
13 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.010 1.000 1 2019 2019
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.010 1.000 1 2013 2013
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.010 1.000 1 2016 2016