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.
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
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
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
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
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
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 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
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
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
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
Neck discomfort
CUI: C0863104
Disease: Neck discomfort
2 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2019 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
Oestrogen receptor positive breast cancer
CUI: C2938924
Disease: 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
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
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
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
progesterone receptor-negative breast cancer
CUI: C4733093
Disease: 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
CUI: C4733094
Disease: 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
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