Source: ALL

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: rs1061539
rs1061539
HLA-A
1.000 0.040 6 29969778 downstream gene variant T/A;C snv
CUI: C0042345
Disease: Varicosity
Varicosity 		0.700 1.000 1 2018 2018
dbSNP: rs1061539
rs1061539
HLA-A
1.000 0.040 6 29969778 downstream gene variant T/A;C snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
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: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		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: rs114577328
rs114577328
HLA-A
1.000 0.080 6 29959505 downstream gene variant G/C snv 1.3E-02
CUI: C0860207
Disease: Drug-Induced Liver Disease
Drug-Induced Liver Disease 		0.010 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: 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: rs1275561861
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		0.010 1.000 1 2014 2014
dbSNP: rs1275561861
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		0.010 1.000 1 2014 2014
dbSNP: rs1275561861
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.010 1.000 1 2004 2004
dbSNP: rs1275561861
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv
CUI: C0276623
Disease: Chronic viral hepatitis
Chronic viral hepatitis 		0.010 1.000 1 2014 2014
dbSNP: rs1275561861
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.010 1.000 1 2002 2002
dbSNP: rs1275561861
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv
CUI: C0020541
Disease: Portal Hypertension
Portal Hypertension 		0.010 1.000 1 2009 2009
dbSNP: rs1275561861
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv
CUI: C1623038
Disease: Cirrhosis
Cirrhosis 		0.010 1.000 1 2014 2014
dbSNP: rs1275561861
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv
CUI: C0022408
Disease: Arthropathy
Arthropathy 		0.010 1.000 1 2014 2014
dbSNP: rs1275561861
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		0.010 1.000 1 2013 2013
dbSNP: rs1275561861
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2014 2014
dbSNP: rs1275561861
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv
CUI: C0011847
Disease: Diabetes
Diabetes 		0.010 1.000 1 2014 2014