Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2107357 16 27399508 upstream gene variant A/G snv 0.85 1
rs2197415 10 9020893 intergenic variant T/G snv 0.66 1
rs2507978 6 31383887 upstream gene variant G/A snv 0.50 1
rs2589561 1.000 0.080 10 9004682 intergenic variant A/G snv 0.83 1
rs28895016 6 31606748 downstream gene variant C/T snv 5.4E-02 1
rs343478 9 6051399 intron variant G/A;C snv 1
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 1
rs4090390 1 173177782 upstream gene variant C/A snv 0.29 1
rs413382 1.000 0.080 9 6142948 intergenic variant C/A snv 0.81 1
rs4801001 18 54668944 intergenic variant T/C snv 0.62 1
rs56129466 11 128288294 intergenic variant A/G snv 0.18 1
rs5758343 22 41420648 intergenic variant A/T snv 0.82 1
rs59593577 11 95692362 intron variant C/T snv 0.12 1
rs6473223 8 80355920 intron variant T/A;C snv 1
rs6869502 5 110830384 intergenic variant A/T snv 0.28 1
rs7032572 9 6172380 intergenic variant A/G snv 0.15 1
rs7127307 1.000 0.120 11 128317488 regulatory region variant T/C snv 0.47 1
rs7130753 11 111599843 upstream gene variant C/T snv 0.37 1
rs7214661 17 45353330 TF binding site variant A/G snv 0.39 1
rs7714574 5 40492553 intron variant C/A;G;T snv 1
rs7720838 0.925 0.040 5 40486794 intron variant G/T snv 0.52 1
rs7741091 6 31384854 upstream gene variant A/G snv 0.36 1
rs7824394 8 80380364 intron variant A/C;T snv 1
rs7927997 1.000 0.040 11 76590331 upstream gene variant C/T snv 0.34 1
rs8069176 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 1