Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2271338 | 0.827 | 0.080 | 4 | 61996533 | intron variant | G/A | snv | 0.26 | 5 | ||
rs5050 | 0.827 | 0.200 | 1 | 230714140 | intron variant | T/C;G | snv | 7 | |||
rs17522122 | 0.925 | 0.040 | 14 | 32833676 | 3 prime UTR variant | G/T | snv | 0.41 | 5 | ||
rs4261436 | 0.925 | 0.040 | 14 | 32830276 | 3 prime UTR variant | T/C | snv | 0.43 | 3 | ||
rs1801516 | 0.627 | 0.400 | 11 | 108304735 | missense variant | G/A | snv | 0.11 | 0.11 | 39 | |
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs137852972 | 0.752 | 0.240 | 11 | 62702499 | missense variant | T/C | snv | 1.6E-05 | 10 | ||
rs773442580 | 0.851 | 0.080 | 4 | 109913367 | missense variant | T/C;G | snv | 4.0E-06 | 7 | ||
rs58064122 | 0.882 | 0.160 | 17 | 44913334 | missense variant | G/A;C | snv | 3 | |||
rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 188 | |
rs121913500 | 0.529 | 0.600 | 2 | 208248388 | missense variant | C/A;G;T | snv | 4.0E-06 | 96 | ||
rs121913499 | 0.605 | 0.520 | 2 | 208248389 | missense variant | G/A;C;T | snv | 51 | |||
rs1040177874 | 0.925 | 0.040 | 2 | 208239914 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
rs118101777 | 0.614 | 0.280 | 15 | 90087472 | missense variant | C/T | snv | 2.0E-03 | 1.6E-03 | 42 | |
rs1801275 | 0.581 | 0.680 | 16 | 27363079 | missense variant | A/G | snv | 0.25 | 0.36 | 58 | |
rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 | |
rs2378456 | 0.807 | 0.200 | 3 | 188885218 | 3 prime UTR variant | C/G;T | snv | 6 | |||
rs7115578 | 0.882 | 0.040 | 11 | 96266936 | intron variant | G/A | snv | 0.37 | 3 | ||
rs2431689 | 0.882 | 0.040 | 5 | 160472115 | intron variant | G/A | snv | 0.17 | 3 | ||
rs3745601 | 0.882 | 0.120 | 19 | 10113872 | missense variant | G/A | snv | 0.16 | 0.13 | 3 | |
rs662 | 0.485 | 0.840 | 7 | 95308134 | missense variant | T/C | snv | 0.38 | 0.42 | 157 | |
rs854560 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 113 | ||
rs6089953 | 0.882 | 0.080 | 20 | 63659655 | intron variant | A/G | snv | 0.82 | 3 | ||
rs6010620 | 0.701 | 0.360 | 20 | 63678486 | intron variant | A/C;G | snv | 21 |