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: rs11221332
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		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: 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: 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: 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: 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: 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: 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