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: rs114811870
rs114811870
HLA-B ; MIR6891
6 31357161 5 prime UTR variant C/T snv 4.2E-02 8.2E-02
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement 		0.700 1.000 1 2019 2019
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: 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: rs2442719
rs2442719
HLA-B
0.882 0.120 6 31352761 intron variant C/T snv 0.53
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2015 2015
dbSNP: rs2523608
rs2523608
HLA-B ; MIR6891
0.925 0.040 6 31354782 non coding transcript exon variant G/A snv 0.19
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.800 1.000 1 2009 2010
dbSNP: rs115392158
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2016 2016
dbSNP: rs115392158
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 1 2016 2016
dbSNP: rs2428494
rs2428494
HLA-B
0.827 0.160 6 31354420 intron variant T/A;C snv
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma 		0.700 1.000 1 2019 2019
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: rs2442719
rs2442719
HLA-B
0.882 0.120 6 31352761 intron variant C/T snv 0.53
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2015 2015
dbSNP: rs2523608
rs2523608
HLA-B ; MIR6891
0.925 0.040 6 31354782 non coding transcript exon variant G/A snv 0.19
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.800 1.000 1 2009 2010
dbSNP: rs2854001
rs2854001
HLA-B ; MIR6891
6 31355235 mature miRNA variant G/A snv 0.18 6.2E-02
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2017 2017
dbSNP: rs2428494
rs2428494
HLA-B
0.827 0.160 6 31354420 intron variant T/A;C snv
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		0.700 1.000 1 2018 2018
dbSNP: rs117486637
rs117486637
HLA-B
1.000 0.040 6 31358156 upstream gene variant T/C snv
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2019 2019
dbSNP: rs17192932
rs17192932
HLA-B
1.000 0.040 6 31354352 intron variant C/G snv 4.9E-02
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2019 2019
dbSNP: rs115429782
rs115429782
HLA-B ; LINC02571 ; LOC112267902
1.000 0.080 6 31297975 intron variant T/C snv
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		0.700 1.000 1 2019 2019
dbSNP: rs12191877
rs12191877
HLA-B
0.851 0.120 6 31285148 intron variant C/T snv 0.12
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		0.700 1.000 1 2015 2015
dbSNP: rs13191343
rs13191343
HLA-B ; HLA-C
1.000 0.080 6 31273332 intron variant C/G;T snv 0.13
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		0.800 1.000 1 2010 2010
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: 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: rs114444221
rs114444221
HLA-B
0.925 0.080 6 31335547 intron variant A/G snv 0.18
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs3190923
rs3190923
HLA-B ; MIR6891
1.000 0.080 6 31356722 synonymous variant C/A;G snv 1.7E-02
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs34437781
rs34437781
HLA-B ; MIR6891
1.000 0.080 6 31357178 5 prime UTR variant C/T snv 1.1E-05; 5.2E-02 1.8E-03
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
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: 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