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
rs10734105 1.000 0.040 10 131373856 intergenic variant G/A;C;T snv 1
rs10789230 1.000 0.040 1 67264945 downstream gene variant G/C;T snv 1
rs10801047 1.000 0.040 1 191590226 intergenic variant A/T snv 0.82 1
rs10975003 0.882 0.080 9 5213687 intergenic variant T/C snv 0.43 1
rs11229030 1.000 0.040 11 57435536 regulatory region variant C/T snv 0.55 1
rs11679753 1.000 0.040 2 62325186 regulatory region variant A/C;G;T snv 1
rs11894081 1.000 0.040 2 5523876 intergenic variant G/T snv 0.57 1
rs1199103 1.000 0.040 10 58187470 downstream gene variant A/C;G snv 1
rs12035082 1.000 0.040 1 172929237 intron variant T/C snv 0.52 1
rs12422544 1.000 0.040 12 40134630 intergenic variant T/C snv 2.7E-02 1
rs12567232 1.000 0.040 1 67262335 downstream gene variant G/A snv 0.27 1
rs12663356 1.000 0.040 6 21430497 intergenic variant T/C snv 0.52 1
rs13073817 1.000 0.040 3 18665366 intron variant G/A;C snv 1
rs13192471 0.925 0.160 6 32703326 downstream gene variant T/C snv 0.19 1
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 1
rs1373692 1.000 0.040 5 40431081 non coding transcript exon variant A/C;T snv 1
rs140068907 1.000 0.040 6 32691666 regulatory region variant A/C snv 3.4E-03 1
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 1
rs147629807 1.000 0.040 5 108553338 intergenic variant T/- del 1
rs1487630 1.000 0.040 4 38334202 intergenic variant C/T snv 0.14 1
rs1495965 0.790 0.280 1 67287825 intergenic variant C/T snv 0.55 1
rs1499555 1.000 0.040 9 22589172 intergenic variant G/A snv 0.36 1
rs17234657 0.882 0.120 5 40401407 intergenic variant T/G snv 0.14 1
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 1