rs2280714, TNPO3

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 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 0.060 1.000 6 2006 2017
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 0.020 1.000 2 2009 2013
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 0.010 1 2009 2009
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 0.010 1.000 1 2018 2018
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 0.010 1.000 1 2018 2018
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
84 0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 0.010 1.000 1 2018 2018
Lymphohistiocytosis, Hemophagocytic
CUI: C0024291
Disease: Lymphohistiocytosis, Hemophagocytic
13 0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 0.010 1.000 1 2011 2011
Macrophage Activation Syndrome
CUI: C1096155
Disease: Macrophage Activation Syndrome
6 0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 0.010 1.000 1 2011 2011
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 0.010 1.000 1 2008 2008
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 0.010 1.000 1 2009 2009