Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs6313 | 0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 | 82 | |
rs25531 | 0.581 | 0.520 | 17 | 30237328 | upstream gene variant | T/C | snv | 0.18 | 72 | ||
rs53576 | 0.641 | 0.320 | 3 | 8762685 | intron variant | A/G;T | snv | 42 | |||
rs6277 | 0.689 | 0.480 | 11 | 113412737 | synonymous variant | G/A | snv | 0.41 | 0.38 | 36 | |
rs165599 | 0.677 | 0.280 | 22 | 19969258 | 3 prime UTR variant | G/A | snv | 0.56 | 27 | ||
rs6354 | 0.732 | 0.280 | 17 | 30222880 | 5 prime UTR variant | G/C;T | snv | 16 | |||
rs578776 | 0.742 | 0.240 | 15 | 78596058 | 3 prime UTR variant | G/A | snv | 0.39 | 13 | ||
rs27072 | 0.807 | 0.120 | 5 | 1394407 | 3 prime UTR variant | C/A;T | snv | 11 | |||
rs737865 | 0.763 | 0.240 | 22 | 19942598 | intron variant | A/G | snv | 0.23 | 11 | ||
rs2020936 | 0.776 | 0.160 | 17 | 30223796 | intron variant | G/A;C | snv | 10 | |||
rs208294 | 0.790 | 0.320 | 12 | 121162450 | missense variant | T/A;C;G | snv | 0.51 | 9 | ||
rs3743078 | 0.807 | 0.160 | 15 | 78602417 | intron variant | C/A;G | snv | 7 | |||
rs2522833 | 0.827 | 0.080 | 7 | 82824392 | missense variant | A/C | snv | 0.45 | 0.34 | 7 | |
rs1106634 | 0.851 | 0.080 | 8 | 20208538 | intron variant | G/A;C;T | snv | 0.18 | 5 | ||
rs680244 | 0.882 | 0.120 | 15 | 78578946 | intron variant | T/C | snv | 0.60 | 4 | ||
rs2609997 | 0.882 | 0.120 | 8 | 56447926 | intron variant | T/C | snv | 0.34 | 3 | ||
rs4965121 | 1.000 | 0.040 | 15 | 97975562 | downstream gene variant | C/A;G | snv | 2 | |||
rs1909884 | 0.925 | 0.120 | 15 | 32147097 | intron variant | G/A | snv | 0.41 | 2 | ||
rs2337980 | 0.925 | 0.120 | 15 | 32151995 | intron variant | C/T | snv | 0.45 | 2 | ||
rs2835731 | 1.000 | 0.040 | 21 | 37424426 | intron variant | C/G;T | snv | 0.17 | 2 | ||
rs9561329 | 1.000 | 0.040 | 13 | 93358916 | intron variant | A/G | snv | 0.15 | 2 |