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: rs8705
rs8705
ETS1
11 128459018 3 prime UTR variant G/A;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs11221357
rs11221357
ETS1 ; LOC105369565
11 128574116 intron variant C/T snv 0.35
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs116502295
rs116502295
ETS1
1.000 11 128462620 intron variant T/C snv 6.1E-03 7.1E-03
CUI: C0869220
Disease: Adverse effects, not elsewhere classified
Adverse effects, not elsewhere classified 		0.700 1.000 1 2019 2019
dbSNP: rs34834119
rs34834119
ETS1
11 128463122 intron variant AT/- del 0.26
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs34834119
rs34834119
ETS1
11 128463122 intron variant AT/- del 0.26
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs4937334
rs4937334
ETS1
11 128465683 intron variant G/A snv 0.22
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs7108992
rs7108992
ETS1
11 128511972 intron variant A/C snv 0.71
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs8705
rs8705
ETS1
11 128459018 3 prime UTR variant G/A;T snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs8705
rs8705
ETS1
11 128459018 3 prime UTR variant G/A;T snv
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs8705
rs8705
ETS1
11 128459018 3 prime UTR variant G/A;T snv
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs8705
rs8705
ETS1
11 128459018 3 prime UTR variant G/A;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs7924522
rs7924522
ETS1
1.000 0.040 11 128510847 intron variant C/A snv 0.70
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 3 2018 2018
dbSNP: rs3802826
rs3802826
ETS1
0.925 0.040 11 128536543 non coding transcript exon variant A/G;T snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.800 1.000 1 2012 2012
dbSNP: rs3802826
rs3802826
ETS1
0.925 0.040 11 128536543 non coding transcript exon variant A/G;T snv
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris 		0.700 1.000 1 2015 2015
dbSNP: rs6590334
rs6590334
ETS1
1.000 0.040 11 128533313 intron variant T/C snv 0.60
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015
dbSNP: rs7924522
rs7924522
ETS1
1.000 0.040 11 128510847 intron variant C/A snv 0.70
CUI: C0017601
Disease: Glaucoma
Glaucoma 		0.700 1.000 1 2018 2018
dbSNP: rs11819995
rs11819995
ETS1
1.000 0.080 11 128519496 intron variant C/T snv 0.23
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2019 2019
dbSNP: rs3809006
rs3809006
ETS1
1.000 0.080 11 128540941 intron variant C/G;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2013 2013
dbSNP: rs4128561
rs4128561
ETS1
1.000 0.080 11 128545234 intron variant T/C snv 0.58
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2016 2016
dbSNP: rs61907765
rs61907765
ETS1 ; MIR6090
1.000 0.080 11 128522042 5 prime UTR variant C/G;T snv 0.17 0.15
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 1 2011 2011
dbSNP: rs67232546
rs67232546
ETS1 ; ETS1-AS1
1.000 0.080 11 128529043 non coding transcript exon variant C/T snv 0.17
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2018 2018
dbSNP: rs11221322
rs11221322
ETS1
0.827 0.120 11 128476898 intron variant T/C snv 0.13
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs11221322
rs11221322
ETS1
0.827 0.120 11 128476898 intron variant T/C snv 0.13
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs11221322
rs11221322
ETS1
0.827 0.120 11 128476898 intron variant T/C snv 0.13
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs11221322
rs11221322
ETS1
0.827 0.120 11 128476898 intron variant T/C snv 0.13
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016