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: rs2888875
rs2888875
THADA
2 43560953 intron variant A/G snv 0.34
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs35590893
rs35590893
THADA
2 43489794 intron variant G/A snv 0.22
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs3764769
rs3764769
THADA
2 43505819 intron variant C/T snv 0.21
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs6708660
rs6708660
THADA
2 43525243 intron variant T/C snv 0.43
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs6732426
rs6732426
THADA
1.000 0.080 2 43360365 intron variant C/T snv 0.54
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017
dbSNP: rs6740322
rs6740322
THADA
1.000 0.040 2 43334790 intron variant A/C snv 0.20
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		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: 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
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: rs7557989
rs7557989
THADA
2 43403518 intron variant C/T snv 0.34
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7557989
rs7557989
THADA
2 43403518 intron variant C/T snv 0.34
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs7590268
rs7590268
THADA
1.000 0.080 2 43312986 intron variant T/G snv 0.22
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		0.800 1.000 1 2010 2012
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: 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: 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: 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: 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: 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: 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