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.
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
Clear-cell metastatic renal cell carcinoma
CUI: C2931852
Disease: 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
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
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
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
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
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
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
Oestrogen receptor positive breast cancer
CUI: C2938924
Disease: 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
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
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
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
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
114 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.020 1.000 2 2016 2019
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
116 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.720 1.000 2 2016 2019
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
157 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.710 1.000 1 2015 2018
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
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
160 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.710 1.000 1 2015 2018
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
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
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
182 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.030 1.000 3 2016 2019
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
193 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.020 1.000 2 2019 2019
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
203 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.030 1.000 3 2016 2019
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
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