rs5010528, HLA-B;HLA-C

N. diseases: 9
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.
Toxic Epidermal Necrolysis
CUI: C0014518
Disease: Toxic Epidermal Necrolysis
29 0.827 0.240 6 31273255 intron variant A/G snv 0.15 0.720 1.000 2 2017 2018
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
526 0.827 0.240 6 31273255 intron variant A/G snv 0.15 0.700 1.000 1 2010 2010
AIDS, PROGRESSION TO
CUI: C1836233
Disease: AIDS, PROGRESSION TO
526 0.827 0.240 6 31273255 intron variant A/G snv 0.15 0.700 1.000 1 2010 2010
HIV Infections
CUI: C0019693
Disease: HIV Infections
142 0.827 0.240 6 31273255 intron variant A/G snv 0.15 0.700 1.000 1 2017 2017
HIV-1, RESISTANCE TO
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
526 0.827 0.240 6 31273255 intron variant A/G snv 0.15 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 0.827 0.240 6 31273255 intron variant A/G snv 0.15 0.700 1.000 1 2010 2010
Stevens-Johnson Syndrome
CUI: C0038325
Disease: Stevens-Johnson Syndrome
16 0.827 0.240 6 31273255 intron variant A/G snv 0.15 0.700 1.000 1 2017 2017
Schwartz-Jampel Syndrome
CUI: C0036391
Disease: Schwartz-Jampel Syndrome
12 0.827 0.240 6 31273255 intron variant A/G snv 0.15 0.020 1.000 2 2017 2018
Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum
CUI: C3658302
Disease: Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum
1 0.827 0.240 6 31273255 intron variant A/G snv 0.15 0.010 1.000 1 2018 2018