Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9264942
rs9264942
HLA-B ; LOC112267902
0.763 0.400 6 31306603 intron variant T/C snv 0.34
CUI: C4016207
Disease: HIV-1 VIREMIA, SUSCEPTIBILITY TO
HIV-1 VIREMIA, SUSCEPTIBILITY TO 		0.700 0
dbSNP: rs12212594
rs12212594
HLA-B
1.000 0.120 6 31333042 intron variant T/C snv 5.3E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.010 < 0.001 1 2014 2014
dbSNP: rs1232620504
rs1232620504
HLA-B
1.000 0.120 6 31354503 missense variant C/T snv
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.010 < 0.001 1 2006 2006
dbSNP: rs281860374
rs281860374
HLA-B ; HLA-C
0.882 0.080 6 31271730 missense variant G/C snv
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.010 < 0.001 1 2002 2002
dbSNP: rs281860374
rs281860374
HLA-B ; HLA-C
0.882 0.080 6 31271730 missense variant G/C snv
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.010 < 0.001 1 2002 2002
dbSNP: rs281860374
rs281860374
HLA-B ; HLA-C
0.882 0.080 6 31271730 missense variant G/C snv
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 < 0.001 1 2002 2002
dbSNP: rs281860391
rs281860391
HLA-B ; HLA-C
0.925 0.080 6 31271690 stop gained C/T snv
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia 		0.010 < 0.001 1 2005 2005
dbSNP: rs281860391
rs281860391
HLA-B ; HLA-C
0.925 0.080 6 31271690 stop gained C/T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 < 0.001 1 2005 2005
dbSNP: rs9266150
rs9266150
HLA-B ; MIR6891
0.925 0.040 6 31356368 missense variant A/C;G;T snv 0.12; 7.9E-05; 3.8E-04
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.010 < 0.001 1 2018 2018
dbSNP: rs9266150
rs9266150
HLA-B ; MIR6891
0.925 0.040 6 31356368 missense variant A/C;G;T snv 0.12; 7.9E-05; 3.8E-04
CUI: C0037284
Disease: Skin lesion
Skin lesion 		0.010 < 0.001 1 2018 2018
dbSNP: rs12191877
rs12191877
HLA-B
0.851 0.120 6 31285148 intron variant C/T snv 0.12
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.830 1.000 5 2009 2015
dbSNP: rs10484554
rs10484554
HLA-B ; LOC112267902
0.807 0.200 6 31306778 intron variant C/T snv 0.12
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.810 1.000 4 2008 2018
dbSNP: rs2524079
rs2524079
HLA-B
6 31274397 intron variant G/A snv 0.44
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.800 1.000 4 2011 2019
dbSNP: rs2074488
rs2074488
HLA-B ; HLA-C
0.925 0.160 6 31272654 intron variant G/T snv 0.13
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2011
dbSNP: rs2428494
rs2428494
HLA-B
0.827 0.160 6 31354420 intron variant T/A;C snv
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 3 2016 2019
dbSNP: rs2894207
rs2894207
HLA-B ; LINC02571
0.882 0.160 6 31295974 intron variant T/C snv 0.20
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.720 1.000 3 2010 2018
dbSNP: rs9468925
rs9468925
HLA-B
0.851 0.040 6 31291060 intron variant G/A snv 0.44
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.820 1.000 3 2010 2012
dbSNP: rs10484554
rs10484554
HLA-B ; LOC112267902
0.807 0.200 6 31306778 intron variant C/T snv 0.12
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.710 1.000 2 2009 2014
dbSNP: rs10484554
rs10484554
HLA-B ; LOC112267902
0.807 0.200 6 31306778 intron variant C/T snv 0.12
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 2 2009 2010
dbSNP: rs10484554
rs10484554
HLA-B ; LOC112267902
0.807 0.200 6 31306778 intron variant C/T snv 0.12
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 2 2009 2010
dbSNP: rs10484554
rs10484554
HLA-B ; LOC112267902
0.807 0.200 6 31306778 intron variant C/T snv 0.12
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 2 2009 2010
dbSNP: rs10484554
rs10484554
HLA-B ; LOC112267902
0.807 0.200 6 31306778 intron variant C/T snv 0.12
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 2 2009 2010
dbSNP: rs12191877
rs12191877
HLA-B
0.851 0.120 6 31285148 intron variant C/T snv 0.12
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 2 2009 2010
dbSNP: rs12191877
rs12191877
HLA-B
0.851 0.120 6 31285148 intron variant C/T snv 0.12
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 2 2009 2010
dbSNP: rs12191877
rs12191877
HLA-B
0.851 0.120 6 31285148 intron variant C/T snv 0.12
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 2 2009 2010