rs3853839, TLR7

N. diseases: 10
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.
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv 0.080 0.875 8 2010 2019
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv 0.020 1.000 2 2014 2018
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv 0.010 1.000 1 2013 2013
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv 0.010 1.000 1 2017 2017
Hand, Foot and Mouth Disease
CUI: C0018572
Disease: Hand, Foot and Mouth Disease
13 0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv 0.010 1.000 1 2019 2019
Pericardial effusion
CUI: C0031039
Disease: Pericardial effusion
10 0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv 0.010 1.000 1 2014 2014
Periodontitis
CUI: C0031099
Disease: Periodontitis
116 0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv 0.010 1.000 1 2019 2019
Pseudohyperkalemia Cardiff
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
60 0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv 0.010 1.000 1 2018 2018
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv 0.010 1.000 1 2010 2010
Secondary malignant neoplasm of colon and/or rectum
CUI: C4721579
Disease: Secondary malignant neoplasm of colon and/or rectum
68 0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv 0.010 1.000 1 2017 2017