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: rs17293632
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs17293632
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs17293632
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs17293632
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2018 2018
dbSNP: rs17294280
rs17294280
SMAD3
0.882 0.120 15 67175947 intron variant A/G snv 0.19
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		0.700 1.000 1 2018 2018
dbSNP: rs17294280
rs17294280
SMAD3
0.882 0.120 15 67175947 intron variant A/G snv 0.19
CUI: C0018621
Disease: Hay fever
Hay fever 		0.700 1.000 1 2014 2014
dbSNP: rs17294280
rs17294280
SMAD3
0.882 0.120 15 67175947 intron variant A/G snv 0.19
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2014 2014
dbSNP: rs2033784
rs2033784
SMAD3
1.000 0.080 15 67157322 intron variant A/G snv 0.35
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs2033784
rs2033784
SMAD3
1.000 0.080 15 67157322 intron variant A/G snv 0.35
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs2033784
rs2033784
SMAD3
1.000 0.080 15 67157322 intron variant A/G snv 0.35
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2018 2018
dbSNP: rs2118611
rs2118611
SMAD3
15 67109128 intron variant T/C snv 0.23
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2019 2019
dbSNP: rs2289261
rs2289261
SMAD3
1.000 0.080 15 67165147 intron variant G/C;T snv 0.61
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs28617673
rs28617673
SMAD3
1.000 0.080 15 67078906 intron variant C/T snv 0.16
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs34445740
rs34445740
SMAD3
0.925 0.080 15 67183426 intron variant -/A delins 0.29
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs34445740
rs34445740
SMAD3
0.925 0.080 15 67183426 intron variant -/A delins 0.29
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.700 1.000 1 2019 2019
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: 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
dbSNP: rs4776342
rs4776342
SMAD3
15 67126053 intron variant A/G snv 0.30
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		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: rs56062135
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.700 1.000 1 2019 2019