rs9469003, LINC01149

N. diseases: 6
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.
Stevens-Johnson Syndrome
CUI: C0038325
Disease: Stevens-Johnson Syndrome
16 0.882 0.160 6 31440051 intron variant T/C snv 0.22 0.800 1.000 1 2011 2011
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
526 0.882 0.160 6 31440051 intron variant T/C snv 0.22 0.700 1.000 1 2009 2009
AIDS, PROGRESSION TO
CUI: C1836233
Disease: AIDS, PROGRESSION TO
526 0.882 0.160 6 31440051 intron variant T/C snv 0.22 0.700 1.000 1 2009 2009
HIV-1, RESISTANCE TO
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
526 0.882 0.160 6 31440051 intron variant T/C snv 0.22 0.700 1.000 1 2009 2009
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
527 0.882 0.160 6 31440051 intron variant T/C snv 0.22 0.700 1.000 1 2009 2009
Toxic Epidermal Necrolysis
CUI: C0014518
Disease: Toxic Epidermal Necrolysis
29 0.882 0.160 6 31440051 intron variant T/C snv 0.22 0.700 1.000 1 2011 2011