Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10276619 1.000 0.080 7 50273756 downstream gene variant G/A snv 0.59 1
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 1
rs10499197 0.925 0.080 6 137811379 intergenic variant T/G snv 2.4E-02 1
rs10903340 1.000 0.080 8 11593078 regulatory region variant T/A;C;G snv 1
rs10911628 1.000 0.080 1 184680369 intergenic variant C/A snv 9.4E-02 1
rs10946940 1.000 0.080 6 27592808 upstream gene variant A/C;G snv 1
rs11117433 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 1
rs11235667 0.925 0.120 11 73152652 intergenic variant A/G snv 2.3E-03 1
rs11655550 1.000 0.080 17 39453870 upstream gene variant T/C snv 0.16 1
rs11697848 1.000 0.080 20 49958778 downstream gene variant C/T snv 3.6E-02 1
rs12068671 0.925 0.160 1 172711891 intergenic variant T/C snv 0.23 1
rs12537284 1.000 0.080 7 129077852 intergenic variant G/A snv 0.11 1
rs12711490 0.925 0.080 16 85939422 intron variant T/C snv 0.18 1
rs13069553 0.851 0.200 3 169790484 upstream gene variant A/G snv 0.21 1
rs13192841 0.925 0.120 6 137646077 intergenic variant G/A snv 0.24 1
rs16840639 0.925 0.120 1 196855643 intron variant T/C snv 0.23 1
rs205284 1.000 0.080 6 34584135 downstream gene variant C/G;T snv 1
rs2061831 0.925 0.160 8 11482373 upstream gene variant T/C snv 0.25 1
rs2084654 1.000 0.080 7 129089074 intergenic variant A/G snv 0.39 1
rs231726 0.790 0.200 2 203876143 downstream gene variant C/T snv 0.36 1
rs2618444 0.925 0.160 8 11480861 intron variant A/C;T snv 1
rs2736332 0.925 0.160 8 11482456 upstream gene variant G/C;T snv 1
rs2736336 0.925 0.160 8 11484361 upstream gene variant G/A;C;T snv 1
rs3129975 1.000 0.080 6 30764277 intron variant T/C;G snv 1
rs4112788 0.851 0.120 1 152578800 downstream gene variant A/G;T snv 1