rs2853676, TERT

N. diseases: 23
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.
Glioma
CUI: C0017638
Disease: Glioma
283 0.667 0.560 5 1288432 intron variant T/A;C snv 0.840 1.000 4 2009 2017
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
183 0.667 0.560 5 1288432 intron variant T/A;C snv 0.020 1.000 2 2014 2015
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 0.667 0.560 5 1288432 intron variant T/A;C snv 0.020 1.000 2 2012 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.667 0.560 5 1288432 intron variant T/A;C snv 0.020 1.000 2 2012 2015
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
167 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2014 2014
Adult type dermatomyositis
CUI: C0221056
Disease: Adult type dermatomyositis
31 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2015 2015
Astrocytoma
CUI: C0004114
Disease: Astrocytoma
51 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2013 2013
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2145 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2019 2019
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
995 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2014 2014
Childhood Astrocytoma
CUI: C4086152
Disease: Childhood Astrocytoma
39 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2013 2013
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
301 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2019 2019
Dermatomyositis
CUI: C0011633
Disease: Dermatomyositis
33 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2015 2015
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
714 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2015 2015
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2019 2019
Idiopathic Pulmonary Fibrosis
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
37 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2019 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
2154 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2019 2019
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1000 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2014 2014
melanoma
CUI: C0025202
Disease: melanoma
352 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2011 2011
MYOTONIC DYSTROPHY 1
CUI: C3250443
Disease: MYOTONIC DYSTROPHY 1
12 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2015 2015
Nicotine Dependence
CUI: C0028043
Disease: Nicotine Dependence
178 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2014 2014
Polymyositis
CUI: C0085655
Disease: Polymyositis
21 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2015 2015
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2014 2014
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
197 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2014 2014