Source: GWASDB

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: rs744910
rs744910
SMAD3
1.000 0.080 15 67154447 intron variant G/A;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.810 1.000 3 2010 2012
dbSNP: rs17228212
rs17228212
SMAD3
0.807 0.160 15 67166301 intron variant T/C snv 0.21
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.810 1.000 2 2007 2012
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: rs17228058
rs17228058
SMAD3
1.000 0.040 15 67157967 intron variant A/G snv 0.17
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.800 1.000 1 2013 2013
dbSNP: rs17293632
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2010 2017
dbSNP: rs17293632
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 1 2012 2017
dbSNP: rs17294280
rs17294280
SMAD3
0.882 0.120 15 67175947 intron variant A/G snv 0.19
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.800 1.000 1 2013 2016
dbSNP: rs16950687
rs16950687
SMAD3
15 67171675 intron variant A/G;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013
dbSNP: rs17293632
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013
dbSNP: rs1866316
rs1866316
SMAD3
15 67149659 intron variant T/C snv 0.36
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013
dbSNP: rs2033784
rs2033784
SMAD3
1.000 0.080 15 67157322 intron variant A/G snv 0.35
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013
dbSNP: rs2278546
rs2278546
SMAD3
15 67174264 intron variant A/G snv 0.34
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013
dbSNP: rs35874463
rs35874463
SMAD3
0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs4562997
rs4562997
SMAD3
15 67165814 intron variant G/A;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013
dbSNP: rs7173698
rs7173698
SMAD3
15 67158555 intron variant A/G snv 0.36
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013
dbSNP: rs7174445
rs7174445
SMAD3
15 67158877 intron variant C/G snv 0.36
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013
dbSNP: rs7181556
rs7181556
SMAD3
15 67184430 intron variant C/G;T snv
CUI: C0524957
Disease: Corneal Topography
Corneal Topography 		0.700 1.000 1 2013 2013
dbSNP: rs8032739
rs8032739
SMAD3
15 67156561 intron variant A/G snv 0.36
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013