rs10069690, TERT

N. diseases: 40
Source: BEFREE ×
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.
Childhood Acute Lymphoblastic Leukemia
259 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 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
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
33 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
714 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2015 2015
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
861 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
12 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
21 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
858 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
246 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
321 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
1571 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
46 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2016 2016
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
995 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
769 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
170 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
160 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
169 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
1000 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2017 2017
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
229 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.710 1.000 1 2016 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
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
95 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2018 2018