rs2269426, TNXB

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.
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.807 0.280 6 32108722 intron variant G/A snv 0.35 0.700 1.000 2 2007 2009
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
526 0.807 0.280 6 32108722 intron variant G/A snv 0.35 0.700 1.000 1 2010 2010
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.807 0.280 6 32108722 intron variant G/A snv 0.35 0.700 1.000 1 2012 2012
AIDS, PROGRESSION TO
CUI: C1836233
Disease: AIDS, PROGRESSION TO
526 0.807 0.280 6 32108722 intron variant G/A snv 0.35 0.700 1.000 1 2010 2010
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.807 0.280 6 32108722 intron variant G/A snv 0.35 0.700 1.000 1 2007 2007
HIV-1, RESISTANCE TO
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
526 0.807 0.280 6 32108722 intron variant G/A snv 0.35 0.700 1.000 1 2010 2010
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
527 0.807 0.280 6 32108722 intron variant G/A snv 0.35 0.700 1.000 1 2010 2010
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.807 0.280 6 32108722 intron variant G/A snv 0.35 0.700 1.000 1 2014 2014
Eosinophilia
CUI: C0014457
Disease: Eosinophilia
23 0.807 0.280 6 32108722 intron variant G/A snv 0.35 0.010 1.000 1 2010 2010
Eosinophilic disorder
CUI: C1306759
Disease: Eosinophilic disorder
22 0.807 0.280 6 32108722 intron variant G/A snv 0.35 0.010 1.000 1 2010 2010