Source: GWASCAT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11583043
rs11583043
1 1.000 0.040 1 101000498 intron variant C/T snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs13107612
rs13107612
5 0.827 0.120 4 101818823 intron variant C/T snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs4851529
rs4851529
5 0.827 0.120 2 102030838 downstream gene variant G/A snv 0.44 0.700 1.000 1 2016 2016
dbSNP: rs10185424
rs10185424
2 0.925 0.040 2 102046427 intron variant T/G snv 0.62 0.710 1.000 1 2015 2016
dbSNP: rs2310173
rs2310173
2 0.925 0.080 2 102047167 intron variant T/C;G snv 0.800 1.000 1 2011 2011
dbSNP: rs871656
rs871656
5 0.827 0.120 2 102154822 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs12987977
rs12987977
5 0.827 0.120 2 102358876 intron variant T/G snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs2075184
rs2075184
14 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 0.700 1.000 1 2015 2015
dbSNP: rs3740415
rs3740415
1 1.000 0.040 10 102472959 3 prime UTR variant G/A snv 0.48 0.48 0.700 1.000 1 2015 2015
dbSNP: rs3774937
rs3774937
5 0.776 0.280 4 102513096 intron variant T/C snv 0.26 0.700 1.000 2 2015 2016
dbSNP: rs3774959
rs3774959
1 0.925 0.080 4 102589957 intron variant G/A snv 0.34 0.800 1.000 1 2012 2012
dbSNP: rs74956615
rs74956615
5 0.807 0.160 19 10317045 3 prime UTR variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs35018800
rs35018800
5 0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 0.700 1.000 1 2016 2016
dbSNP: rs12720356
rs12720356
7 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 0.700 1.000 2 2015 2016
dbSNP: rs62131887
rs62131887
14 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 0.700 1.000 1 2015 2015
dbSNP: rs35074907
rs35074907
6 0.807 0.160 19 10489742 synonymous variant G/A snv 1.9E-02 1.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs2189234
rs2189234
3 1.000 0.040 4 105154341 intron variant T/G snv 0.62 0.700 1.000 1 2015 2015
dbSNP: rs10010325
rs10010325
3 1.000 0.040 4 105185196 intron variant C/A;G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs11750385
rs11750385
5 0.827 0.120 5 10521556 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs7746082
rs7746082
3 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs4946717
rs4946717
6 0.827 0.120 6 106026874 intron variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs6911490
rs6911490
1 1.000 0.040 6 106074152 intron variant T/C snv 0.86 0.800 1.000 1 2011 2011
dbSNP: rs28701841
rs28701841
5 0.827 0.120 6 106082455 intron variant G/A snv 7.6E-02 0.700 1.000 1 2016 2016
dbSNP: rs11839053
rs11839053
14 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs12369214
rs12369214
5 0.807 0.120 12 106804833 intron variant G/A snv 0.41 0.700 1.000 1 2016 2016