Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 1
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 1
rs10500264 1.000 0.080 19 33259408 intergenic variant G/A snv 0.14 1
rs10866713 1.000 0.080 5 159491886 intron variant G/A snv 0.16 1
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 1
rs11129295 1.000 0.080 3 27747289 intergenic variant C/T snv 0.39 1
rs12048904 1.000 0.080 1 100865980 intergenic variant T/C snv 0.48 1
rs12087340 1.000 0.080 1 85281310 intron variant C/T snv 8.4E-02 1
rs12296430 1.000 0.080 12 6394334 splice region variant G/C snv 0.16 1
rs13192841 0.925 0.120 6 137646077 intergenic variant G/A snv 0.24 1
rs13333054 1.000 0.080 16 85977427 intron variant C/A;T snv 1
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 1
rs17066096 1.000 0.080 6 137131771 intergenic variant A/G snv 0.20 1
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 1
rs1843938 1.000 0.080 7 3073400 intergenic variant G/A snv 0.42 1
rs201847125 1.000 0.080 7 50285971 intergenic variant C/T snv 1
rs2082412 0.925 0.120 5 159290781 downstream gene variant G/A snv 0.27 1
rs2163226 1.000 0.080 2 43134117 upstream gene variant T/C snv 0.33 1
rs2182410 1.000 0.080 10 6080706 intergenic variant T/A;C snv 1
rs233100 1.000 0.080 1 85306326 intron variant G/A snv 0.40 1
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 1
rs2744148 1.000 0.080 16 1023552 intergenic variant A/G snv 0.15 1
rs2920001 1.000 0.080 18 31209762 intergenic variant T/C snv 0.20 1
rs3129889 1.000 0.080 6 32445768 downstream gene variant G/A;T snv 1
rs3135338 0.882 0.240 6 32433440 regulatory region variant C/T snv 0.62 1