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: rs3869062
rs3869062
HLA-A
1.000 0.120 6 29967114 downstream gene variant A/G snv 5.5E-02
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.720 1.000 5 2009 2017
dbSNP: rs2517713
rs2517713
HLA-A
1.000 0.120 6 29950322 downstream gene variant G/A;T snv
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.710 1.000 4 2009 2015
dbSNP: rs12206499
rs12206499
HLA-A
1.000 0.040 6 29969350 downstream gene variant A/G snv 0.27
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 2 2011 2012
dbSNP: rs417162
rs417162
HLA-A
1.000 0.120 6 29948728 downstream gene variant C/T snv 0.66
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 1.000 2 2009 2012
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: 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: 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: rs150881176
rs150881176
HLA-A
1.000 0.120 6 29979963 downstream gene variant T/C snv
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis 		0.700 1.000 1 2016 2016
dbSNP: rs1632879
rs1632879
HLA-A
6 29949926 downstream gene variant G/A snv 0.82
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs1632883
rs1632883
HLA-A
6 29948216 downstream gene variant C/A snv 0.78
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs1655900
rs1655900
HLA-A
1.000 0.080 6 29948841 downstream gene variant G/A snv 0.14
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.700 1.000 1 2012 2012
dbSNP: rs1655900
rs1655900
HLA-A
1.000 0.080 6 29948841 downstream gene variant G/A snv 0.14
CUI: C0729353
Disease: Subfertility
Subfertility 		0.010 1.000 1 2016 2016
dbSNP: rs1655902
rs1655902
HLA-A
1.000 0.080 6 29949078 downstream gene variant G/A;C snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.700 1.000 1 2011 2011
dbSNP: rs1655904
rs1655904
HLA-A
6 29949369 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: rs192543598
rs192543598
HLA-A
6 29963568 downstream gene variant A/G snv 1.6E-02
CUI: C2004491
Disease: Cicatrix
Cicatrix 		0.700 1.000 1 2019 2019
dbSNP: rs192543598
rs192543598
HLA-A
6 29963568 downstream gene variant A/G snv 1.6E-02
CUI: C1869024
Disease: Severe cutaneous adverse reactions (SMQ)
Severe cutaneous adverse reactions (SMQ) 		0.700 1.000 1 2019 2019
dbSNP: rs2256543
rs2256543
HLA-A
0.925 0.080 6 29970056 downstream gene variant T/C snv 0.59
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 1 2009 2009
dbSNP: rs2256543
rs2256543
HLA-A
0.925 0.080 6 29970056 downstream gene variant T/C snv 0.59
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.700 1.000 1 2009 2009