rs1805034, TNFRSF11A

N. diseases: 12
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.
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 0.010 1.000 1 2014 2014
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 0.010 1.000 1 2014 2014
Gastric Cardia Adenocarcinoma
CUI: C1333762
Disease: Gastric Cardia Adenocarcinoma
11 0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 0.010 1.000 1 2015 2015
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 0.010 1.000 1 2015 2015
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 0.010 1.000 1 2014 2014
Osteitis Deformans
CUI: C0029401
Disease: Osteitis Deformans
58 0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 0.010 1.000 1 2012 2012
Osteoarthritis, Knee
CUI: C0409959
Disease: Osteoarthritis, Knee
150 0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 0.010 1.000 1 2019 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 0.010 1 2019 2019
Root Resorption
CUI: C0035851
Disease: Root Resorption
7 0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 0.010 1.000 1 2014 2014
Secondary malignant neoplasm of bone
18 0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 0.010 1.000 1 2014 2014
Squamous cell carcinoma of esophagus
329 0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 0.010 1.000 1 2014 2014
Urticaria
CUI: C0042109
Disease: Urticaria
11 0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 0.010 1.000 1 2015 2015