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: rs9260620
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs9260620
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs9260620
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs9260620
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs9260620
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs9260620
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs9260620
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs9260489
rs9260489
HLA-A
1.000 0.080 6 29952555 upstream gene variant T/A;G snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs9260489
rs9260489
HLA-A
1.000 0.080 6 29952555 upstream gene variant T/A;G snv
CUI: C0201910
Disease: Beta-2-microglobulin measurement
Beta-2-microglobulin measurement 		0.800 1.000 1 2013 2013
dbSNP: rs9260313
rs9260313
HLA-A
6 29949108 downstream gene variant T/C snv 0.42
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs9260313
rs9260313
HLA-A
6 29949108 downstream gene variant T/C snv 0.42
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs9260151
rs9260151
HLA-A
1.000 0.120 6 29943253 non coding transcript exon variant C/T snv 0.16 0.14
CUI: C0202100
Disease: Insulin C-peptide measurement
Insulin C-peptide measurement 		0.700 1.000 1 2018 2018
dbSNP: rs9260151
rs9260151
HLA-A
1.000 0.120 6 29943253 non coding transcript exon variant C/T snv 0.16 0.14
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.720 0.500 1 2018 2020
dbSNP: rs9259819
rs9259819
HLA-A ; HCG4B
6 29925798 upstream gene variant G/T snv 0.49
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2017 2017
dbSNP: rs7758512
rs7758512
HLA-A ; ZNRD1ASP
1.000 6 30002812 intron variant T/G snv 0.17
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.800 1.000 1 2009 2009
dbSNP: rs7758512
rs7758512
HLA-A ; ZNRD1ASP
1.000 6 30002812 intron variant T/G snv 0.17
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.800 1.000 1 2009 2009
dbSNP: rs7758512
rs7758512
HLA-A ; ZNRD1ASP
1.000 6 30002812 intron variant T/G snv 0.17
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.800 1.000 1 2009 2009
dbSNP: rs7758512
rs7758512
HLA-A ; ZNRD1ASP
1.000 6 30002812 intron variant T/G snv 0.17
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.800 1.000 1 2009 2009
dbSNP: rs7749944
rs7749944
HLA-A
0.925 6 29992223 upstream gene variant A/C snv 1.3E-02
CUI: C1274700
Disease: Postmenopausal frontal fibrosing alopecia
Postmenopausal frontal fibrosing alopecia 		0.700 1.000 1 2019 2019
dbSNP: rs7749944
rs7749944
HLA-A
0.925 6 29992223 upstream gene variant A/C snv 1.3E-02
CUI: C4255374
Disease: Frontal fibrosing alopecia
Frontal fibrosing alopecia 		0.700 1.000 1 2019 2019
dbSNP: rs6914699
rs6914699
HLA-A
6 29966245 downstream gene variant T/C snv 0.41
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs60131261
rs60131261
HLA-A
1.000 0.040 6 29969559 downstream gene variant TTTA/- delins 0.26
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2016 2016
dbSNP: rs4313034
rs4313034
HLA-A ; HLA-J ; ZNRD1ASP
0.925 0.160 6 30006148 non coding transcript exon variant C/T snv 0.78
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer 		0.700 1.000 1 2019 2019
dbSNP: rs4313034
rs4313034
HLA-A ; HLA-J ; ZNRD1ASP
0.925 0.160 6 30006148 non coding transcript exon variant C/T snv 0.78
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.800 1.000 1 2011 2011
dbSNP: rs41546314
rs41546314
HLA-A
1.000 0.040 6 29942601 synonymous variant C/T snv 0.26
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer 		0.700 1.000 1 2019 2019