rs2853676, TERT

N. diseases: 29
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.
Glioma
CUI: C0017638
Disease: Glioma
353 0.667 0.560 5 1288432 intron variant T/A;C snv 0.840 1.000 6 2009 2017
Central Nervous System Neoplasms
CUI: C0085136
Disease: Central Nervous System Neoplasms
72 0.667 0.560 5 1288432 intron variant T/A;C snv 0.700 1.000 1 2009 2009
Lung Diseases, Interstitial
CUI: C0206062
Disease: Lung Diseases, Interstitial
144 0.667 0.560 5 1288432 intron variant T/A;C snv 0.700 1.000 1 2013 2013
Malignant Testicular Germ Cell Tumor
62 0.667 0.560 5 1288432 intron variant T/A;C snv 0.700 1.000 1 2010 2010
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.667 0.560 5 1288432 intron variant T/A;C snv 0.700 1.000 1 2010 2010
Plexiform leiomyoma
CUI: C2242776
Disease: Plexiform leiomyoma
103 0.667 0.560 5 1288432 intron variant T/A;C snv 0.700 1.000 1 2019 2019
Uterine Fibroids
CUI: C0042133
Disease: Uterine Fibroids
154 0.667 0.560 5 1288432 intron variant T/A;C snv 0.700 1.000 1 2019 2019
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 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
1641 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
168 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
59 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
2793 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
1204 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
852 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2019 2019
Dermatomyositis
CUI: C0011633
Disease: Dermatomyositis
34 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
824 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
63 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
3417 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
1142 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2014 2014
melanoma
CUI: C0025202
Disease: melanoma
515 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
14 0.667 0.560 5 1288432 intron variant T/A;C snv 0.010 1.000 1 2015 2015