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: rs13429458
rs13429458
THADA
0.827 0.200 2 43411699 intron variant A/C snv 0.14
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.890 0.800 2 2011 2019
dbSNP: rs7578597
rs7578597
THADA
0.807 0.240 2 43505684 missense variant T/C snv 9.9E-02 0.14
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.840 1.000 2 2008 2017
dbSNP: rs12478601
rs12478601
THADA
0.851 0.200 2 43494369 intron variant C/T snv 0.61
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.820 0.750 1 2011 2019
dbSNP: rs10495903
rs10495903
THADA
1.000 0.040 2 43579779 intron variant C/T snv 0.13
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 3 2010 2017
dbSNP: rs10495903
rs10495903
THADA
1.000 0.040 2 43579779 intron variant C/T snv 0.13
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 2 2012 2017
dbSNP: rs10203174
rs10203174
THADA
1.000 0.080 2 43462891 intron variant C/T snv 0.17
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.800 1.000 1 2012 2012
dbSNP: rs17030845
rs17030845
THADA
2 43460740 intron variant C/T snv 0.11
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.800 1.000 1 2011 2011
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: rs1465618
rs1465618
THADA
0.882 0.160 2 43326810 intron variant T/C snv 0.80
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.720 0.800 3 2009 2019
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: rs7563201
rs7563201
THADA
1.000 0.120 2 43334641 intron variant G/A snv 0.45
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.700 1.000 2 2015 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: rs11694173
rs11694173
THADA
0.827 0.080 2 43363760 intron variant G/A snv 0.14
CUI: C2676272
Disease: Alopecia, Androgenetic, 3
Alopecia, Androgenetic, 3 		0.700 1.000 1 2016 2016
dbSNP: rs11694173
rs11694173
THADA
0.827 0.080 2 43363760 intron variant G/A snv 0.14
CUI: C0029489
Disease: Other alopecia
Other alopecia 		0.700 1.000 1 2016 2016
dbSNP: rs11694173
rs11694173
THADA
0.827 0.080 2 43363760 intron variant G/A snv 0.14
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.700 1.000 1 2016 2016
dbSNP: rs11694173
rs11694173
THADA
0.827 0.080 2 43363760 intron variant G/A snv 0.14
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
Alopecia, Androgenetic, 1 		0.700 1.000 1 2016 2016
dbSNP: rs11694173
rs11694173
THADA
0.827 0.080 2 43363760 intron variant G/A snv 0.14
CUI: C2678038
Disease: Alopecia, Androgenetic, 2
Alopecia, Androgenetic, 2 		0.700 1.000 1 2016 2016
dbSNP: rs11694173
rs11694173
THADA
0.827 0.080 2 43363760 intron variant G/A snv 0.14
CUI: C0162311
Disease: Androgenetic Alopecia
Androgenetic Alopecia 		0.700 1.000 1 2016 2016
dbSNP: rs11694173
rs11694173
THADA
0.827 0.080 2 43363760 intron variant G/A snv 0.14
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs13405158
rs13405158
THADA
1.000 0.080 2 43478147 intron variant T/C snv 0.17
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2012 2012
dbSNP: rs13414381
rs13414381
THADA
1.000 0.080 2 43340079 intron variant T/C snv 0.18
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2019 2019
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