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: 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: rs11221332
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2017 2017
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: rs11221332
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
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: 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: 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: 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: 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