rs10069690, TERT

N. diseases: 53
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.
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.750 1.000 8 2011 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.750 1.000 11 2011 2019
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.700 1.000 2 2018 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2016 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.020 1.000 2 2013 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.020 1.000 2 2013 2019
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2017 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2017 2017
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.700 1.000 1 2019 2019
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2015 2015
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2017 2017
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2015 2015
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2017 2017
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2019 2019
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2015 2015
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.710 1.000 2 2016 2017
Glioma
CUI: C0017638
Disease: Glioma
353 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.700 1.000 3 2015 2018
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2016 2016
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.020 1.000 2 2015 2016
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.800 1.000 2 2013 2019
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.030 1.000 3 2016 2019
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.710 1.000 3 2015 2018
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2017 2017
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2017 2017
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2013 2013