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: rs111312615
rs111312615
HLA-A
1.000 0.040 6 29955302 upstream gene variant T/G snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs113205291
rs113205291
HLA-A
1.000 0.040 6 29894844 upstream gene variant A/G;T snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs113205291
rs113205291
HLA-A
1.000 0.040 6 29894844 upstream gene variant A/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs114204022
rs114204022
HLA-A
1.000 0.040 6 29972902 upstream gene variant G/A snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs114204022
rs114204022
HLA-A
1.000 0.040 6 29972902 upstream gene variant G/A snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs114577328
rs114577328
HLA-A
1.000 0.080 6 29959505 downstream gene variant G/C snv 1.3E-02
CUI: C4277682
Disease: Chemical and Drug Induced Liver Injury
Chemical and Drug Induced Liver Injury 		0.700 1.000 1 2017 2017
dbSNP: rs114950038
rs114950038
HLA-A
1.000 0.040 6 29983056 downstream gene variant G/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs114950038
rs114950038
HLA-A
1.000 0.040 6 29983056 downstream gene variant G/A;C snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs115625073
rs115625073
HLA-A ; HCG4B
1.000 0.040 6 29924456 upstream gene variant T/C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs115625073
rs115625073
HLA-A ; HCG4B
1.000 0.040 6 29924456 upstream gene variant T/C snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs115729734
rs115729734
HLA-A
1.000 0.080 6 29931238 upstream gene variant T/C;G snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.700 1.000 1 2017 2017
dbSNP: rs115960997
rs115960997
HLA-A
1.000 0.040 6 29934332 downstream gene variant G/A;T snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs115960997
rs115960997
HLA-A
1.000 0.040 6 29934332 downstream gene variant G/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs144304366
rs144304366
HLA-A
1.000 0.040 6 29936216 downstream gene variant T/C snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs144304366
rs144304366
HLA-A
1.000 0.040 6 29936216 downstream gene variant T/C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs147097402
rs147097402
HLA-A
1.000 0.080 6 29930083 upstream gene variant C/A;G;T snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.700 1.000 1 2017 2017
dbSNP: rs3094146
rs3094146
HLA-A ; ZNRD1ASP
1.000 0.080 6 30003183 non coding transcript exon variant G/C snv 6.1E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
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