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: rs3771180
rs3771180
1.000 0.080 2 102337157 5 prime UTR variant G/A;T snv
CUI: C0004096
Disease: Asthma
Asthma
0.820 1.000 2 2011 2019
dbSNP: rs10197862
rs10197862
0.925 0.120 2 102350089 intron variant A/G snv 0.18
CUI: C0004096
Disease: Asthma
Asthma
0.810 1.000 1 2011 2014
dbSNP: rs13015714
rs13015714
0.882 0.200 2 102355405 intron variant G/T snv 0.77
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.810 1.000 1 2008 2009
dbSNP: rs13408661
rs13408661
1.000 0.080 2 102338622 intron variant G/A snv 0.18
CUI: C0004096
Disease: Asthma
Asthma
0.810 1.000 1 2011 2012
dbSNP: rs3771166
rs3771166
1.000 0.080 2 102369762 intron variant G/A;T snv
CUI: C0004096
Disease: Asthma
Asthma
0.810 1.000 1 2010 2012
dbSNP: rs13015714
rs13015714
0.882 0.200 2 102355405 intron variant G/T snv 0.77
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.800 1.000 2 2012 2015
dbSNP: rs1420101
rs1420101
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.800 1.000 1 2009 2009
dbSNP: rs950881
rs950881
1.000 0.120 2 102316052 intron variant G/A;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.800 1.000 1 2013 2016
dbSNP: rs9807989
rs9807989
1.000 0.080 2 102354740 intron variant T/C;G snv 0.46
CUI: C0004096
Disease: Asthma
Asthma
0.800 1.000 1 2012 2012
dbSNP: rs1420101
rs1420101
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35
CUI: C0004096
Disease: Asthma
Asthma
0.710 1.000 2 2018 2019
dbSNP: rs1420101
rs1420101
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35
CUI: C0027430
Disease: Nasal Polyps
Nasal Polyps
0.710 0.500 1 2010 2019
dbSNP: rs72823641
rs72823641
0.882 0.080 2 102319699 intron variant T/A;C snv
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 3 2018 2019
dbSNP: rs10208293
rs10208293
0.882 0.160 2 102349850 intron variant G/A snv 0.33
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 2 2016 2019
dbSNP: rs72823641
rs72823641
0.882 0.080 2 102319699 intron variant T/A;C snv
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.700 1.000 2 2019 2019
dbSNP: rs10197862
rs10197862
0.925 0.120 2 102350089 intron variant A/G snv 0.18
CUI: C0018621
Disease: Hay fever
Hay fever
0.700 1.000 1 2014 2014
dbSNP: rs10208293
rs10208293
0.882 0.160 2 102349850 intron variant G/A snv 0.33
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.700 1.000 1 2019 2019
dbSNP: rs10865050
rs10865050
2 102324851 intron variant G/A snv 0.18
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2017 2017
dbSNP: rs11465606
rs11465606
2 102371840 intron variant C/A snv 1.6E-02
CUI: C4268744
Disease: Atypical femoral fracture
Atypical femoral fracture
0.700 1.000 1 2019 2019
dbSNP: rs11676124
rs11676124
2 102324878 intron variant T/C snv 0.66
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs12479210
rs12479210
1.000 0.080 2 102332701 intron variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs12712135
rs12712135
2 102314488 intron variant A/G snv 0.55
Interleukin 1 Receptor-Like 1 Measurement
0.700 1.000 1 2017 2017
dbSNP: rs12987977
rs12987977
0.827 0.120 2 102358876 intron variant T/G snv 0.31
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2016 2016
dbSNP: rs12987977
rs12987977
0.827 0.120 2 102358876 intron variant T/G snv 0.31
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2016 2016
dbSNP: rs12987977
rs12987977
0.827 0.120 2 102358876 intron variant T/G snv 0.31
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2016 2016
dbSNP: rs12987977
rs12987977
0.827 0.120 2 102358876 intron variant T/G snv 0.31
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016