Source: GWASCAT

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: 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 3 2008 2018
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: 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 3 2011 2019
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 2 2009 2015
dbSNP: rs2247056
rs2247056
HLA-B ; LINC02571 ; LOC112267902
0.882 0.160 6 31297713 intron variant T/C snv 0.80
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2010 2018
dbSNP: rs2524079
rs2524079
HLA-B
6 31274397 intron variant G/A snv 0.44
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 2 2011 2017
dbSNP: rs2853946
rs2853946
HLA-B
6 31279426 intron variant A/G;T snv 0.37
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 2 2014 2019
dbSNP: rs2894207
rs2894207
HLA-B ; LINC02571
0.882 0.160 6 31295974 intron variant T/C snv 0.20
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
Nasopharyngeal Neoplasms 		0.700 1.000 2 2010 2016
dbSNP: rs3819299
rs3819299
HLA-B
1.000 6 31354590 non coding transcript exon variant T/G snv 7.7E-02 2.3E-02
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.800 1.000 2 2011 2016
dbSNP: rs9264942
rs9264942
HLA-B ; LOC112267902
0.763 0.400 6 31306603 intron variant T/C snv 0.34
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.800 1.000 2 2009 2010
dbSNP: rs9264942
rs9264942
HLA-B ; LOC112267902
0.763 0.400 6 31306603 intron variant T/C snv 0.34
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 2 2012 2015
dbSNP: rs9264942
rs9264942
HLA-B ; LOC112267902
0.763 0.400 6 31306603 intron variant T/C snv 0.34
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.800 1.000 2 2009 2010
dbSNP: rs9264942
rs9264942
HLA-B ; LOC112267902
0.763 0.400 6 31306603 intron variant T/C snv 0.34
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.800 1.000 2 2009 2010
dbSNP: rs9264942
rs9264942
HLA-B ; LOC112267902
0.763 0.400 6 31306603 intron variant T/C snv 0.34
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.800 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: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		0.800 1.000 1 2009 2009
dbSNP: rs1050529
rs1050529
HLA-B ; MIR6891
0.882 0.040 6 31356838 missense variant C/T snv 0.11
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs1050529
rs1050529
HLA-B ; MIR6891
0.882 0.040 6 31356838 missense variant C/T snv 0.11
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs1050529
rs1050529
HLA-B ; MIR6891
0.882 0.040 6 31356838 missense variant C/T snv 0.11
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.700 1.000 1 2016 2016
dbSNP: rs1065386
rs1065386
HLA-B ; MIR6891
1.000 0.160 6 31356770 missense variant G/A;C;T snv 0.34; 5.6E-06
CUI: C0154830
Disease: Proliferative diabetic retinopathy
Proliferative diabetic retinopathy 		0.700 1.000 1 2019 2019
dbSNP: rs1071816
rs1071816
HLA-B ; MIR6891
1.000 0.040 6 31356759 missense variant T/A;C;G snv 0.30; 0.16; 0.34; 2.7E-02
CUI: C0272178
Disease: Drug-induced neutropenia
Drug-induced neutropenia 		0.700 1.000 1 2016 2016
dbSNP: rs1093
rs1093
HLA-B
1.000 0.080 6 31354129 3 prime UTR variant A/G snv 0.15
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs1131275
rs1131275
HLA-B ; MIR6891
1.000 0.040 6 31356183 missense variant G/A;C snv 0.68
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs1131275
rs1131275
HLA-B ; MIR6891
1.000 0.040 6 31356183 missense variant G/A;C snv 0.68
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs1140404
rs1140404
HLA-B ; MIR6891
6 31356750 missense variant T/C;G snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs114208039
rs114208039
HLA-B ; HLA-C
6 31273862 intron variant A/G snv
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2018 2018