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: rs72743461
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 3 2019 2019
dbSNP: rs12901372
rs12901372
SMAD3
1.000 0.040 15 67078168 intron variant C/A;G snv
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip 		0.700 1.000 2 2018 2019
dbSNP: rs72743461
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 2 2017 2018
dbSNP: rs10152595
rs10152595
SMAD3
1.000 0.080 15 67183150 intron variant C/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs10152595
rs10152595
SMAD3
1.000 0.080 15 67183150 intron variant C/G;T snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs11639295
rs11639295
SMAD3
1.000 0.040 15 67168419 intron variant C/G;T snv
CUI: C0339682
Disease: Regular astigmatism - corneal
Regular astigmatism - corneal 		0.700 1.000 1 2018 2018
dbSNP: rs12913547
rs12913547
SMAD3
15 67175169 intron variant T/C;G snv
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs12913547
rs12913547
SMAD3
15 67175169 intron variant T/C;G snv
CUI: C0524957
Disease: Corneal Topography
Corneal Topography 		0.800 1.000 1 2013 2013
dbSNP: rs35251008
rs35251008
SMAD3
15 67176187 intron variant A/C;G snv
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs4776879
rs4776879
SMAD3
15 67071982 intron variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs72743461
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.700 1.000 1 2019 2019
dbSNP: rs72743461
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.700 1.000 1 2015 2015
dbSNP: rs72743461
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs72743461
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma 		0.700 1.000 1 2019 2019
dbSNP: rs72743481
rs72743481
SMAD3
15 67173209 intron variant T/A;C snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs744910
rs744910
SMAD3
1.000 0.080 15 67154447 intron variant G/A;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.810 1.000 1 2010 2012
dbSNP: rs8025774
rs8025774
SMAD3
15 67190938 3 prime UTR variant C/G;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2018 2018
dbSNP: rs117683492
rs117683492
SMAD3
1.000 0.080 15 67121286 intron variant G/A snv 1.2E-02
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs35874463
rs35874463
SMAD3
0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2017 2019
dbSNP: rs35874463
rs35874463
SMAD3
0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs35874463
rs35874463
SMAD3
0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs35874463
rs35874463
SMAD3
0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs35874463
rs35874463
SMAD3
0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs35874463
rs35874463
SMAD3
0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs35874463
rs35874463
SMAD3
0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		0.700 1.000 1 2019 2019