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: 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
dbSNP: rs2394250
rs2394250
HLA-A ; HCG9
1.000 0.040 6 29975879 intron variant G/T snv 0.40
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2013 2013
dbSNP: rs2517713
rs2517713
HLA-A
1.000 0.120 6 29950322 downstream gene variant G/A;T snv
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
Nasopharyngeal Neoplasms 		0.700 1.000 1 2009 2009
dbSNP: rs2517873
rs2517873
HLA-A ; MCCD1P1
1.000 0.080 6 29908215 intron variant G/A snv 0.15
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs2523933
rs2523933
HLA-A
6 29964515 intergenic variant G/C;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs2523961
rs2523961
HLA-A ; MICD
0.925 0.120 6 29971803 non coding transcript exon variant G/A snv 0.16
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2018 2018
dbSNP: rs2523961
rs2523961
HLA-A ; MICD
0.925 0.120 6 29971803 non coding transcript exon variant G/A snv 0.16
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.700 1.000 1 2018 2018
dbSNP: rs2524005
rs2524005
HLA-A
0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2012 2012
dbSNP: rs2524005
rs2524005
HLA-A
0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2012 2012
dbSNP: rs2571400
rs2571400
HLA-A
6 29959945 downstream gene variant C/G snv 0.51
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs28749114
rs28749114
HLA-A
6 29937675 upstream gene variant A/G;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2975009
rs2975009
HLA-A
6 29930339 upstream gene variant C/T snv 0.50
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
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: rs3132685
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018