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: rs17228212
rs17228212
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 1 2007 2012
dbSNP: rs744910
rs744910
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: rs17293632
rs17293632
0.763 0.240 15 67150258 intron variant C/T snv 0.17
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 4 2010 2017
dbSNP: rs17293632
rs17293632
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 3 2012 2017
dbSNP: rs12913547
rs12913547
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
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: rs17294280
rs17294280
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: rs56062135
rs56062135
0.790 0.200 15 67163292 intron variant C/T snv 0.18
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.710 1.000 2 2015 2018
dbSNP: rs17293632
rs17293632
0.763 0.240 15 67150258 intron variant C/T snv 0.17
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 3 2015 2017
dbSNP: rs72743461
rs72743461
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
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: rs35874463
rs35874463
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: rs72743461
rs72743461
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
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
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: rs10438355
rs10438355
15 67195211 downstream gene variant C/G snv 0.20
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs11071939
rs11071939
15 67171053 intron variant T/C snv 6.1E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2019 2019
dbSNP: rs11639295
rs11639295
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: rs117683492
rs117683492
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: rs12901071
rs12901071
0.882 0.160 15 67078051 intron variant A/G snv 0.25
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip
0.700 1.000 1 2018 2018
dbSNP: rs12912010
rs12912010
15 67174805 intron variant G/T snv 0.24
CUI: C1720164
Disease: Central corneal thickness
Central corneal thickness
0.700 1.000 1 2018 2018
dbSNP: rs12912045
rs12912045
15 67174959 intron variant C/T snv 0.25
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2017 2017
dbSNP: rs12913547
rs12913547
15 67175169 intron variant T/C;G snv
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018
dbSNP: rs17228058
rs17228058
1.000 0.040 15 67157967 intron variant A/G snv 0.17
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2018 2018
dbSNP: rs17293632
rs17293632
0.763 0.240 15 67150258 intron variant C/T snv 0.17
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016