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 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
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
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
progesterone receptor-negative breast cancer
11 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2013 2013
progesterone receptor-positive breast cancer
17 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2013 2013
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
Adult type dermatomyositis
CUI: C0221056
Disease: Adult type dermatomyositis
31 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2015 2015
Dermatomyositis
CUI: C0011633
Disease: Dermatomyositis
34 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2015 2015
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
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
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
MYOTONIC DYSTROPHY 1
CUI: C3250443
Disease: MYOTONIC DYSTROPHY 1
14 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2015 2015
Polymyositis
CUI: C0085655
Disease: Polymyositis
22 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2015 2015
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
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
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
Clear-cell metastatic renal cell carcinoma
11 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2016 2016
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
Oestrogen receptor positive breast cancer
58 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2016 2016
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
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
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
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