rs12153855, TNXB

N. diseases: 10
Source: GWASDB ×
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.
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
279 0.776 0.320 6 32107027 intron variant T/C snv 0.11 0.820 1.000 1 2012 2016
Dermatitis, Atopic
CUI: C0011615
Disease: Dermatitis, Atopic
47 0.776 0.320 6 32107027 intron variant T/C snv 0.11 0.800 1.000 1 2013 2013
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
365 0.776 0.320 6 32107027 intron variant T/C snv 0.11 0.700 1.000 2 2009 2010
AIDS, PROGRESSION TO
CUI: C1836233
Disease: AIDS, PROGRESSION TO
365 0.776 0.320 6 32107027 intron variant T/C snv 0.11 0.700 1.000 2 2009 2010
HIV-1, RESISTANCE TO
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
365 0.776 0.320 6 32107027 intron variant T/C snv 0.11 0.700 1.000 2 2009 2010
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
365 0.776 0.320 6 32107027 intron variant T/C snv 0.11 0.700 1.000 2 2009 2010
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
1613 0.776 0.320 6 32107027 intron variant T/C snv 0.11 0.700 1.000 2 2007 2009
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
477 0.776 0.320 6 32107027 intron variant T/C snv 0.11 0.700 1.000 1 2007 2007
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
78 0.776 0.320 6 32107027 intron variant T/C snv 0.11 0.700 1.000 1 2010 2010
Vitiligo
CUI: C0042900
Disease: Vitiligo
121 0.776 0.320 6 32107027 intron variant T/C snv 0.11 0.700 1.000 1 2010 2010