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.
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
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
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
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
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
Central Nervous System Neoplasms
CUI: C0085136
Disease: Central Nervous System Neoplasms
72 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.700 1.000 2 2015 2017
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
Epithelial ovarian cancer
CUI: C0677886
Disease: Epithelial ovarian cancer
129 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.700 1.000 1 2015 2015
Lung Diseases, Interstitial
CUI: C0206062
Disease: Lung Diseases, Interstitial
144 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.700 1.000 1 2013 2013
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
Malignant Testicular Germ Cell Tumor
CUI: C0855197
Disease: Malignant Testicular Germ Cell Tumor
62 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.700 1.000 1 2010 2010
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
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
Small Lymphocytic Lymphoma
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
122 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.700 1.000 1 2019 2019
Triple Negative Breast Neoplasms
CUI: C3539878
Disease: Triple Negative Breast Neoplasms
99 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.700 1.000 1 2014 2014
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
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
estrogen receptor-negative breast cancer
CUI: C4733092
Disease: estrogen receptor-negative breast cancer
40 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.020 1.000 2 2011 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
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