Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13022699 1.000 0.080 2 101671373 intergenic variant C/T snv 5.3E-02 1
rs12468899 1.000 0.080 2 101809678 intron variant A/G;T snv 1
rs1709393 1.000 0.080 3 101980310 intron variant C/T snv 0.55 2
rs13427957 1.000 0.080 2 102072571 intron variant C/T snv 0.46 1
rs74180212 0.925 0.080 2 102181785 intron variant T/C;G snv 2
rs10189629 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 1
rs78545931 0.925 0.080 2 102265892 intergenic variant A/G snv 0.16 2
rs60227565 0.925 0.080 2 102275879 intergenic variant G/A;T snv 0.10 2
rs202011557 1.000 0.080 2 102297182 intergenic variant -/CAA delins 1
rs10515922 1.000 0.080 2 102298194 regulatory region variant A/G snv 6.9E-02 1
rs12470864 0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30 4
rs72823641 0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs12479210 1.000 0.080 2 102332701 intron variant C/A;T snv 1
rs3771180 1.000 0.080 2 102337157 5 prime UTR variant G/A;T snv 1
rs13408661 1.000 0.080 2 102338622 intron variant G/A snv 0.18 1
rs1420101 0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 3
rs3771175 0.925 0.080 2 102343750 3 prime UTR variant T/A snv 0.18 1
rs10208293 0.882 0.160 2 102349850 intron variant G/A snv 0.33 2
rs10197862 0.925 0.120 2 102350089 intron variant A/G snv 0.18 2
rs1861245 0.925 0.080 2 102350446 intron variant C/T snv 2
rs9807989 1.000 0.080 2 102354740 intron variant T/C;G snv 0.46 2
rs3771166 1.000 0.080 2 102369762 intron variant G/A;T snv 1
rs2241116 1.000 0.080 2 102386805 intron variant C/A;T snv 1
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 2
rs227283 0.925 0.120 4 102686096 intron variant C/G;T snv 2