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: 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: rs2523946
rs2523946
HLA-A ; HCG9
0.925 0.200 6 29974166 upstream gene variant C/A;G;T snv
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis 		0.800 1.000 2 2011 2015
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: rs2860580
rs2860580
HLA-A
1.000 0.120 6 29938914 upstream gene variant A/C;G;T snv
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
Nasopharyngeal Neoplasms 		0.700 1.000 2 2010 2016
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
dbSNP: rs3823355
rs3823355
HLA-A ; HCG9
1.000 0.040 6 29974306 upstream gene variant C/A;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 1 2010 2010
dbSNP: rs3893463
rs3893463
HLA-A
6 29967628 downstream gene variant C/T snv 0.41
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs3893464
rs3893464
HLA-A
1.000 0.120 6 29967473 downstream gene variant G/A snv 0.46
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs3893464
rs3893464
HLA-A
1.000 0.120 6 29967473 downstream gene variant G/A snv 0.46
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.800 1.000 1 2011 2011
dbSNP: rs3893464
rs3893464
HLA-A
1.000 0.120 6 29967473 downstream gene variant G/A snv 0.46
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs41546314
rs41546314
HLA-A
1.000 0.040 6 29942601 synonymous variant C/T snv 0.26
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer 		0.700 1.000 1 2019 2019
dbSNP: rs4313034
rs4313034
HLA-A ; HLA-J ; ZNRD1ASP
0.925 0.160 6 30006148 non coding transcript exon variant C/T snv 0.78
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer 		0.700 1.000 1 2019 2019
dbSNP: rs4313034
rs4313034
HLA-A ; HLA-J ; ZNRD1ASP
0.925 0.160 6 30006148 non coding transcript exon variant C/T snv 0.78
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.800 1.000 1 2011 2011
dbSNP: rs60131261
rs60131261
HLA-A
1.000 0.040 6 29969559 downstream gene variant TTTA/- delins 0.26
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2016 2016
dbSNP: rs6914699
rs6914699
HLA-A
6 29966245 downstream gene variant T/C snv 0.41
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018