Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11688000 | 1.000 | 0.040 | 2 | 75066030 | intron variant | A/G | snv | 0.34 | 1 | ||
rs10948172 | 0.882 | 0.040 | 6 | 44809954 | intron variant | A/G | snv | 0.27 | 3 | ||
rs2979715 | 1.000 | 0.040 | 8 | 79650024 | intron variant | C/T | snv | 0.77 | 1 | ||
rs2228314 | 0.790 | 0.360 | 22 | 41880738 | missense variant | G/C | snv | 0.34 | 0.38 | 8 | |
rs1042667 | 1.000 | 0.040 | 17 | 72124410 | 3 prime UTR variant | A/C | snv | 0.41 | 0.36 | 3 | |
rs12601701 | 1.000 | 0.040 | 17 | 72119217 | intron variant | G/A | snv | 0.35 | 1 | ||
rs1566347 | 1.000 | 0.040 | 4 | 185811412 | intron variant | T/C | snv | 0.69 | 1 | ||
rs11177 | 0.851 | 0.080 | 3 | 52687289 | missense variant | G/A | snv | 0.38 | 0.33 | 4 | |
rs12901071 | 0.882 | 0.160 | 15 | 67078051 | intron variant | A/G | snv | 0.25 | 3 | ||
rs12901499 | 0.882 | 0.040 | 15 | 67078107 | intron variant | G/A | snv | 0.45 | 3 | ||
rs2289263 | 0.925 | 0.120 | 15 | 67146869 | intron variant | T/G | snv | 0.43 | 3 | ||
rs6494629 | 0.925 | 0.120 | 15 | 67081773 | intron variant | C/T | snv | 0.52 | 2 | ||
rs12102171 | 1.000 | 0.040 | 15 | 67132695 | intron variant | C/T | snv | 0.22 | 1 | ||
rs12595334 | 1.000 | 0.040 | 15 | 67192818 | 3 prime UTR variant | C/T | snv | 0.19 | 1 | ||
rs3743342 | 1.000 | 0.040 | 15 | 67193329 | 3 prime UTR variant | C/T | snv | 0.20 | 1 | ||
rs8031440 | 1.000 | 0.040 | 15 | 67191641 | 3 prime UTR variant | G/A | snv | 0.19 | 1 | ||
rs1560707 | 1.000 | 0.040 | 19 | 10640062 | intron variant | T/A;G | snv | 1 | |||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 34 | ||
rs764256352 | 0.882 | 0.120 | 5 | 149981625 | missense variant | G/C | snv | 4.0E-06 | 2.1E-05 | 3 | |
rs1052981 | 1.000 | 0.040 | 7 | 37906899 | 3 prime UTR variant | G/A | snv | 0.70 | 1 | ||
rs1127379 | 0.882 | 0.120 | 8 | 41263761 | 3 prime UTR variant | T/C | snv | 0.48 | 3 | ||
rs528981060 | 1.000 | 0.040 | 22 | 43266235 | intron variant | G/A | snv | 5.0E-04 | 1 | ||
rs62174901 | 1.000 | 0.040 | 2 | 165131833 | intron variant | T/C | snv | 0.12 | 1 | ||
rs62174906 | 1.000 | 0.040 | 2 | 165151847 | intron variant | A/G | snv | 0.13 | 1 | ||
rs6746030 | 0.763 | 0.320 | 2 | 166242648 | missense variant | A/G | snv | 0.88 | 0.88 | 16 |