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: rs116392568
rs116392568
HLA-B ; LOC112267902
1.000 0.040 6 31306603 intron variant T/C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2015 2015
dbSNP: rs116392568
rs116392568
HLA-B ; LOC112267902
1.000 0.040 6 31306603 intron variant T/C snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs12111032
rs12111032
HLA-B
1.000 0.080 6 31274414 intron variant A/G snv 0.23
CUI: C0039263
Disease: Takayasu Arteritis
Takayasu Arteritis 		0.700 1.000 1 2015 2015
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: rs148203517
rs148203517
HLA-B ; MIR6891
1.000 0.120 6 31356323 missense variant G/A;T snv
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		0.700 1.000 1 2015 2015
dbSNP: rs2442719
rs2442719
HLA-B
0.882 0.120 6 31352761 intron variant C/T snv 0.53
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2015 2015
dbSNP: rs2442719
rs2442719
HLA-B
0.882 0.120 6 31352761 intron variant C/T snv 0.53
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection 		0.700 1.000 1 2015 2015
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: rs2442719
rs2442719
HLA-B
0.882 0.120 6 31352761 intron variant C/T snv 0.53
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2015 2015
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: rs2596500
rs2596500
HLA-B
0.925 0.120 6 31353490 intron variant A/C;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2015 2015
dbSNP: rs4406273
rs4406273
HLA-B ; LINC02571 ; LOC112267902
0.925 0.040 6 31298313 intron variant G/A snv 8.6E-02
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris 		0.700 1.000 1 2015 2015
dbSNP: rs6919908
rs6919908
HLA-B ; USP8P1
0.882 0.160 6 31277183 non coding transcript exon variant T/C snv 0.83
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		0.700 1.000 1 2015 2015
dbSNP: rs6919908
rs6919908
HLA-B ; USP8P1
0.882 0.160 6 31277183 non coding transcript exon variant T/C snv 0.83
CUI: C0026470
Disease: Monoclonal Gammopathy of Undetermined Significance
Monoclonal Gammopathy of Undetermined Significance 		0.700 1.000 1 2015 2015
dbSNP: rs6919908
rs6919908
HLA-B ; USP8P1
0.882 0.160 6 31277183 non coding transcript exon variant T/C snv 0.83
CUI: C0030489
Disease: Paraproteinemias
Paraproteinemias 		0.700 1.000 1 2015 2015
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: 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: 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: rs111721712
rs111721712
HLA-B
6 31347630 intron variant -/T delins 0.55
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs114985235
rs114985235
HLA-B ; LINC02571 ; LOC112267902
1.000 0.040 6 31301916 intron variant T/C snv 6.0E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.710 1.000 1 2016 2016
dbSNP: rs115392158
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs115392158
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2016 2016