| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11893432 | 0.827 | 0.120 | 2 | 191057148 | intron variant | C/G | snv | 0.21 | 5 | ||
| rs10919563 | 0.925 | 0.120 | 1 | 198731313 | intron variant | G/A | snv | 0.21 | 3 | ||
| rs1003706636 | 1.000 | 0.120 | 1 | 247424639 | missense variant | T/C | snv | 1 | |||
| rs10128264 | 1.000 | 0.120 | 10 | 79200216 | intron variant | T/C | snv | 0.64 | 1 | ||
| rs1018981 | 1.000 | 0.120 | 7 | 41335525 | intergenic variant | C/A | snv | 3.2E-02 | 1 | ||
| rs10431961 | 1.000 | 0.120 | 16 | 3050094 | synonymous variant | C/G;T | snv | 4.0E-06; 0.32 | 1 | ||
| rs10761744 | 1.000 | 0.120 | 10 | 63341266 | intron variant | C/G;T | snv | 0.87 | 1 | ||
| rs10956445 | 1.000 | 0.120 | 8 | 128775730 | intron variant | T/C | snv | 0.20 | 1 | ||
| rs11225055 | 1.000 | 0.120 | 11 | 101900702 | intron variant | T/A;C | snv | 1 | |||
| rs11817689 | 1.000 | 0.120 | 10 | 63164457 | downstream gene variant | T/C | snv | 0.13 | 1 | ||
| rs12002949 | 1.000 | 0.120 | 9 | 1469317 | intergenic variant | G/A | snv | 0.16 | 1 | ||
| rs12046117 | 1.000 | 0.120 | 1 | 117208743 | intron variant | C/T | snv | 0.16 | 1 | ||
| rs12411988 | 1.000 | 0.120 | 10 | 63555637 | intron variant | G/C | snv | 0.12 | 1 | ||
| rs12416113 | 1.000 | 0.120 | 10 | 63136717 | intron variant | T/A | snv | 0.13 | 1 | ||
| rs12652364 | 1.000 | 0.120 | 5 | 30835972 | intergenic variant | G/A;T | snv | 1 | |||
| rs12719740 | 1.000 | 0.120 | 15 | 98529676 | intron variant | G/A | snv | 0.21 | 1 | ||
| rs16918575 | 1.000 | 0.120 | 10 | 63541565 | intron variant | A/G | snv | 0.13 | 1 | ||
| rs16939895 | 1.000 | 0.120 | 18 | 12821904 | intron variant | G/A | snv | 0.17 | 1 | ||
| rs2294369 | 1.000 | 0.120 | 22 | 39679395 | missense variant | G/A | snv | 0.23 | 0.17 | 1 | |
| rs2893922 | 1.000 | 0.120 | 10 | 63487259 | intron variant | T/C;G | snv | 1 | |||
| rs4395908 | 1.000 | 0.120 | 8 | 4168122 | intron variant | C/A;G | snv | 1 | |||
| rs4688011 | 1.000 | 0.120 | 3 | 119508400 | intron variant | G/A;C | snv | 0.15 | 1 | ||
| rs4746201 | 1.000 | 0.120 | 10 | 63562621 | intron variant | G/A;T | snv | 2.2E-05; 0.16 | 1 | ||
| rs6479891 | 1.000 | 0.120 | 10 | 63246696 | intron variant | T/A;C | snv | 1 | |||
| rs7082090 | 1.000 | 0.120 | 10 | 63239252 | intron variant | A/G | snv | 0.87 | 1 |