Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2847281 | 1.000 | 0.040 | 18 | 12821594 | intron variant | A/G | snv | 0.32 | 3 | ||
rs7309332 | 1.000 | 0.040 | 12 | 7938243 | upstream gene variant | T/C | snv | 0.59 | 3 | ||
rs74664507 | 1.000 | 0.040 | 9 | 16913838 | upstream gene variant | T/A | snv | 3 | |||
rs1047325 | 1.000 | 0.040 | 1 | 153561551 | missense variant | C/T | snv | 7.1E-02 | 0.16 | 2 | |
rs10759637 | 1.000 | 0.040 | 9 | 113262744 | 3 prime UTR variant | A/C | snv | 0.47 | 2 | ||
rs121913082 | 1.000 | 0.040 | 10 | 89014205 | missense variant | A/G | snv | 2 | |||
rs121913083 | 1.000 | 0.040 | 10 | 89008907 | missense variant | A/G | snv | 2 | |||
rs121913084 | 1.000 | 0.040 | 10 | 89010779 | missense variant | T/C | snv | 2 | |||
rs1670661 | 1.000 | 0.040 | 11 | 21209124 | intron variant | C/G;T | snv | 2 | |||
rs17761864 | 1.000 | 0.040 | 17 | 2268343 | intron variant | C/A | snv | 0.28 | 2 | ||
rs2239612 | 1.000 | 0.040 | 3 | 187075454 | intron variant | G/A | snv | 0.17 | 2 | ||
rs4785204 | 1.000 | 0.040 | 16 | 50069823 | intron variant | C/T | snv | 8.6E-02 | 2 | ||
rs6413464 | 1.000 | 0.040 | 9 | 21970980 | missense variant | C/A;G | snv | 1.3E-03; 4.1E-06 | 2 | ||
rs6503659 | 1.000 | 0.040 | 17 | 41741012 | intergenic variant | A/C;G;T | snv | 2 | |||
rs1064793400 | 1.000 | 0.040 | 3 | 37048550 | missense variant | G/A | snv | 1 | |||
rs1064793981 | 1.000 | 0.040 | 2 | 47475030 | missense variant | G/A | snv | 1 | |||
rs1078305 | 1.000 | 0.040 | 9 | 121289122 | intron variant | A/G | snv | 0.70 | 1 | ||
rs10818524 | 1.000 | 0.040 | 9 | 121267901 | intron variant | T/C | snv | 0.37 | 1 | ||
rs10971638 | 1.000 | 0.040 | 9 | 33674679 | non coding transcript exon variant | C/T | snv | 0.21 | 1 | ||
rs115169993 | 1.000 | 0.040 | 1 | 162772032 | missense variant | G/A | snv | 7.8E-04 | 2.9E-03 | 1 | |
rs116150891 | 1.000 | 0.040 | 9 | 21970929 | missense variant | G/A;C | snv | 5.6E-04 | 2.6E-03 | 1 | |
rs11707807 | 1.000 | 0.040 | 3 | 188370473 | intron variant | A/G | snv | 0.36 | 1 | ||
rs117984432 | 1.000 | 0.040 | 16 | 89388583 | intron variant | T/C | snv | 2.0E-02 | 1 | ||
rs121913230 | 1.000 | 0.040 | 7 | 55181437 | missense variant | G/A | snv | 1 | |||
rs121913431 | 1.000 | 0.040 | 7 | 55181438 | missense variant | G/A | snv | 1 |