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.
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
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2017 2017
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
Ovarian Serous Adenocarcinoma
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
65 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.700 1.000 1 2017 2017
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
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
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.710 1.000 3 2015 2018
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
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2018 2018
Plexiform leiomyoma
CUI: C2242776
Disease: Plexiform leiomyoma
103 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.700 1.000 1 2018 2018
Uterine Fibroids
CUI: C0042133
Disease: Uterine Fibroids
154 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.700 1.000 1 2018 2018
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
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
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.030 1.000 3 2016 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
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.720 1.000 3 2016 2019
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
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.020 1.000 2 2016 2019
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
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.020 1.000 2 2019 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
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
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.020 1.000 2 2016 2019
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
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2019 2019