Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2186607 | 0.776 | 0.080 | 11 | 101785666 | intron variant | T/A | snv | 0.51 | 10 | ||
rs4450168 | 0.790 | 0.080 | 11 | 10265208 | intron variant | A/C;T | snv | 0.12 | 9 | ||
rs4919687 | 0.742 | 0.160 | 10 | 102835491 | non coding transcript exon variant | G/A | snv | 0.25 | 14 | ||
rs12548629 | 0.776 | 0.120 | 8 | 103189173 | intron variant | C/T | snv | 0.24 | 10 | ||
rs141752671 | 0.708 | 0.280 | 11 | 103745837 | intron variant | A/G | snv | 5.4E-03 | 17 | ||
rs148883465 | 0.708 | 0.280 | 11 | 103813371 | intron variant | A/G | snv | 7.2E-03 | 17 | ||
rs17035289 | 0.790 | 0.080 | 4 | 105127134 | intergenic variant | T/C | snv | 0.25 | 9 | ||
rs7679673 | 0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 | 28 | ||
rs17035310 | 0.790 | 0.080 | 4 | 105143597 | upstream gene variant | C/T | snv | 0.14 | 10 | ||
rs1391441 | 0.763 | 0.240 | 4 | 105207603 | intron variant | G/A | snv | 0.70 | 11 | ||
rs6928864 | 0.790 | 0.080 | 6 | 105519019 | intron variant | C/A;T | snv | 9 | |||
rs1512436 | 0.790 | 0.080 | 11 | 106436144 | intergenic variant | T/C | snv | 0.50 | 10 | ||
rs1078643 | 0.776 | 0.080 | 17 | 10803924 | missense variant | G/A;C | snv | 10 | |||
rs9583269 | 0.790 | 0.080 | 13 | 108630682 | intron variant | C/T | snv | 0.34 | 9 | ||
rs7993934 | 0.790 | 0.080 | 13 | 110422568 | intron variant | C/T | snv | 0.56 | 9 | ||
rs8000189 | 0.776 | 0.080 | 13 | 110423534 | intron variant | C/T | snv | 0.61 | 10 | ||
rs9481067 | 0.776 | 0.080 | 6 | 110429349 | intron variant | A/G | snv | 0.58 | 10 | ||
rs10980628 | 0.776 | 0.080 | 9 | 110909123 | intron variant | T/C | snv | 0.16 | 10 | ||
rs4849303 | 0.790 | 0.080 | 2 | 110970905 | intron variant | C/G;T | snv | 9 | |||
rs3087967 | 0.776 | 0.080 | 11 | 111286111 | 3 prime UTR variant | T/C | snv | 0.72 | 10 | ||
rs3802842 | 0.695 | 0.280 | 11 | 111300984 | intron variant | C/A | snv | 0.71 | 25 | ||
rs6589219 | 0.790 | 0.080 | 11 | 111302186 | intron variant | G/C | snv | 0.69 | 9 | ||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 92 | ||
rs597808 | 0.742 | 0.200 | 12 | 111535554 | intron variant | A/G | snv | 0.67 | 19 | ||
rs121918464 | 0.708 | 0.440 | 12 | 112450406 | missense variant | G/A;C | snv | 25 |