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: rs35720761
rs35720761
THADA
1.000 0.080 2 43292838 missense variant C/A;G;T snv 2.9E-05; 9.9E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2018 2018
dbSNP: rs6743071
rs6743071
THADA
1.000 0.080 2 43359148 intron variant T/C;G snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2018 2018
dbSNP: rs67584485
rs67584485
THADA
2 43535056 intron variant A/C;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs77533229
rs77533229
THADA
2 43252499 intron variant G/A snv 1.8E-02
CUI: C0201983
Disease: Dehydroepiandrosterone sulfate measurement (procedure)
Dehydroepiandrosterone sulfate measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs77059113
rs77059113
THADA
2 43445369 intron variant T/G snv 4.5E-02
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs77981966
rs77981966
THADA
0.827 0.120 2 43550825 intron variant C/T snv 4.6E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs77981966
rs77981966
THADA
0.827 0.120 2 43550825 intron variant C/T snv 4.6E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs77981966
rs77981966
THADA
0.827 0.120 2 43550825 intron variant C/T snv 4.6E-02
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs77981966
rs77981966
THADA
0.827 0.120 2 43550825 intron variant C/T snv 4.6E-02
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs77981966
rs77981966
THADA
0.827 0.120 2 43550825 intron variant C/T snv 4.6E-02
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs113542380
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 3 2018 2018
dbSNP: rs113542380
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs113542380
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs113542380
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs113542380
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs77972916
rs77972916
THADA
2 43534973 intron variant G/A snv 4.7E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs78487399
rs78487399
THADA
2 43582208 intron variant G/C snv 6.2E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs78487399
rs78487399
THADA
2 43582208 intron variant G/C snv 6.2E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs78487399
rs78487399
THADA
2 43582208 intron variant G/C snv 6.2E-02
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs78487399
rs78487399
THADA
2 43582208 intron variant G/C snv 6.2E-02
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs78487399
rs78487399
THADA
2 43582208 intron variant G/C snv 6.2E-02
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs17334919
rs17334919
THADA
1.000 0.080 2 43480246 intron variant C/T snv 7.0E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2018 2018
dbSNP: rs7591387
rs7591387
THADA
2 43528893 intron variant C/T snv 0.10
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs77881454
rs77881454
THADA
2 43530154 intron variant A/T snv 0.11
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs6752964
rs6752964
THADA
2 43527516 intron variant T/C snv 0.11
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2018 2018