Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs188096 | 1.000 | 0.080 | 13 | 103052694 | missense variant | A/C | snv | 0.85 | 0.89 | 1 | |
rs7229639 | 0.763 | 0.080 | 18 | 48924606 | intron variant | A/G | snv | 0.87 | 5 | ||
rs2278008 | 0.851 | 0.160 | 5 | 33989413 | missense variant | C/T | snv | 0.70 | 0.74 | 4 | |
rs3087967 | 0.776 | 0.080 | 11 | 111286111 | 3 prime UTR variant | T/C | snv | 0.72 | 1 | ||
rs25487 | 0.441 | 0.800 | 19 | 43551574 | missense variant | T/C | snv | 0.68 | 0.71 | 205 | |
rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 140 | ||
rs1391441 | 0.763 | 0.240 | 4 | 105207603 | intron variant | G/A | snv | 0.70 | 1 | ||
rs4779584 | 0.732 | 0.160 | 15 | 32702555 | intergenic variant | T/C | snv | 0.67 | 8 | ||
rs10808555 | 0.925 | 0.080 | 8 | 127397266 | intron variant | G/A | snv | 0.65 | 5 | ||
rs1126667 | 0.776 | 0.280 | 17 | 6999441 | missense variant | A/G | snv | 0.60 | 0.62 | 8 | |
rs7013278 | 0.776 | 0.080 | 8 | 127402647 | intron variant | T/C | snv | 0.59 | 1 | ||
rs704017 | 0.776 | 0.080 | 10 | 79059375 | intron variant | A/G | snv | 0.55 | 1 | ||
rs13251096 | 1.000 | 0.080 | 8 | 58505225 | downstream gene variant | A/G | snv | 0.53 | 1 | ||
rs11874392 | 0.763 | 0.080 | 18 | 48926786 | intron variant | A/T | snv | 0.50 | 2 | ||
rs3789243 | 0.776 | 0.120 | 7 | 87591570 | intron variant | A/G | snv | 0.50 | 14 | ||
rs7023329 | 0.790 | 0.160 | 9 | 21816529 | intron variant | A/G | snv | 0.50 | 8 | ||
rs2735940 | 0.689 | 0.400 | 5 | 1296371 | upstream gene variant | A/G | snv | 0.49 | 14 | ||
rs10246939 | 0.851 | 0.240 | 7 | 141972804 | missense variant | T/C | snv | 0.49 | 0.47 | 4 | |
rs1726866 | 0.925 | 0.120 | 7 | 141972905 | missense variant | G/A | snv | 0.50 | 0.47 | 2 | |
rs713598 | 0.851 | 0.160 | 7 | 141973545 | missense variant | C/G | snv | 0.46 | 0.44 | 6 | |
rs4444235 | 0.701 | 0.240 | 14 | 53944201 | downstream gene variant | T/C | snv | 0.43 | 15 | ||
rs10505477 | 0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 | 19 | ||
rs8050136 | 0.716 | 0.560 | 16 | 53782363 | intron variant | C/A | snv | 0.40 | 18 | ||
rs6983267 | 0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 | 55 | ||
rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 187 |