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: rs7183955
rs7183955
0.925 0.080 15 60757370 intron variant A/C snv 0.24
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs7183955
rs7183955
0.925 0.080 15 60757370 intron variant A/C snv 0.24
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma
0.700 1.000 1 2019 2019
dbSNP: rs11071558
rs11071558
1.000 0.080 15 60777222 intron variant A/C;G snv
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2018 2018
dbSNP: rs4775367
rs4775367
15 61169252 intron variant A/C;G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 1 2018 2018
dbSNP: rs12916023
rs12916023
15 61163854 intron variant A/G snv 0.47
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs2028122
rs2028122
0.851 0.120 15 60549076 intron variant A/G snv 0.51
CUI: C0002170
Disease: Alopecia
Alopecia
0.700 1.000 1 2017 2017
dbSNP: rs2899663
rs2899663
15 60902035 intron variant A/G snv 0.49
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs4775300
rs4775300
15 60819119 intron variant A/G snv 5.2E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs339969
rs339969
15 60591082 intron variant C/A snv 0.68
Serum gamma-glutamyl transferase measurement
0.800 1.000 2 2011 2018
dbSNP: rs339969
rs339969
15 60591082 intron variant C/A snv 0.68
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs17270446
rs17270446
15 60781603 intron variant C/G snv 0.28
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs2414679
rs2414679
15 60687613 intron variant C/G snv 0.40
Serum gamma-glutamyl transferase measurement
0.700 1.000 1 2019 2019
dbSNP: rs813017
rs813017
15 61117896 intron variant C/G snv 0.43
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs8035549
rs8035549
15 61032506 intron variant C/G;T snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs11071559
rs11071559
0.925 0.080 15 60777789 intron variant C/T snv 0.23
CUI: C0004096
Disease: Asthma
Asthma
0.820 1.000 3 2010 2019
dbSNP: rs11071559
rs11071559
0.925 0.080 15 60777789 intron variant C/T snv 0.23
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.700 1.000 2 2019 2019
dbSNP: rs11071559
rs11071559
0.925 0.080 15 60777789 intron variant C/T snv 0.23
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases
0.700 1.000 1 2019 2019
dbSNP: rs11071559
rs11071559
0.925 0.080 15 60777789 intron variant C/T snv 0.23
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs12912233
rs12912233
0.851 0.120 15 60974897 intron variant C/T snv 0.38
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2010 2010
dbSNP: rs168144
rs168144
15 60622063 intron variant C/T snv 0.57
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs340029
rs340029
15 60602766 intron variant C/T snv 0.70
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 1 2011 2011
dbSNP: rs340030
rs340030
15 60603943 intron variant C/T snv 0.43
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs10519068
rs10519068
0.925 0.120 15 60776505 intron variant G/A snv 0.22
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 2 2016 2019
dbSNP: rs340005
rs340005
15 60585831 intron variant G/A snv 0.67
Serum gamma-glutamyl transferase measurement
0.800 1.000 2 2012 2019
dbSNP: rs340005
rs340005
15 60585831 intron variant G/A snv 0.67
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 2 2016 2018