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: 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: rs111312615
rs111312615
HLA-A
1.000 0.040 6 29955302 upstream gene variant T/G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2017 2019
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: rs115559990
rs115559990
HLA-A ; HLA-K ; HCG4B
6 29926633 non coding transcript exon variant C/G;T snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
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: rs115928623
rs115928623
HLA-A ; MICD
1.000 0.080 6 29971371 intron variant A/T snv
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		0.700 1.000 1 2019 2019
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: 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: rs16896742
rs16896742
HLA-A
6 29954963 upstream gene variant A/G snv 0.35
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2014 2014
dbSNP: rs17882753
rs17882753
HLA-A
6 29944817 non coding transcript exon variant C/T snv 1.4E-02
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
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: 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