rs2075786, TERT

N. diseases: 8
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.
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
995 0.790 0.360 5 1266195 intron variant A/G snv 0.55 0.010 1.000 1 2009 2009
Hereditary Nonpolyposis Colorectal Cancer
CUI: C1333990
Disease: Hereditary Nonpolyposis Colorectal Cancer
91 0.790 0.360 5 1266195 intron variant A/G snv 0.55 0.010 1.000 1 2013 2013
Lynch Syndrome
CUI: C4552100
Disease: Lynch Syndrome
65 0.790 0.360 5 1266195 intron variant A/G snv 0.55 0.010 1.000 1 2013 2013
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1000 0.790 0.360 5 1266195 intron variant A/G snv 0.55 0.010 1.000 1 2009 2009
Neoplasms
CUI: C0027651
Disease: Neoplasms
1571 0.790 0.360 5 1266195 intron variant A/G snv 0.55 0.010 1.000 1 2013 2013
Paranoid Schizophrenia
CUI: C0036349
Disease: Paranoid Schizophrenia
23 0.790 0.360 5 1266195 intron variant A/G snv 0.55 0.010 1.000 1 2016 2016
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.790 0.360 5 1266195 intron variant A/G snv 0.55 0.010 1.000 1 2009 2009
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
676 0.790 0.360 5 1266195 intron variant A/G snv 0.55 0.010 1.000 1 2017 2017