rs2844511, None

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.
Acquired Immunodeficiency Syndrome
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
42 0.807 0.200 6 31422007 intron variant A/G;T snv 0.700 1.000 1 2009 2009
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
526 0.807 0.200 6 31422007 intron variant A/G;T snv 0.700 1.000 1 2009 2009
AIDS, PROGRESSION TO
CUI: C1836233
Disease: AIDS, PROGRESSION TO
526 0.807 0.200 6 31422007 intron variant A/G;T snv 0.700 1.000 1 2009 2009
HIV-1, RESISTANCE TO
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
526 0.807 0.200 6 31422007 intron variant A/G;T snv 0.700 1.000 1 2009 2009
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
527 0.807 0.200 6 31422007 intron variant A/G;T snv 0.700 1.000 1 2009 2009
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.807 0.200 6 31422007 intron variant A/G;T snv 0.700 1.000 1 2014 2014
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.807 0.200 6 31422007 intron variant A/G;T snv 0.700 1.000 1 2009 2009
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.807 0.200 6 31422007 intron variant A/G;T snv 0.010 1.000 1 2017 2017
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.807 0.200 6 31422007 intron variant A/G;T snv 0.010 1.000 1 2017 2017
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.807 0.200 6 31422007 intron variant A/G;T snv 0.010 1.000 1 2017 2017