| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs585362 | 1 | 109247173 | upstream gene variant | C/G;T | snv | 4 | |||||
| rs611917 | 1.000 | 0.040 | 1 | 109272630 | non coding transcript exon variant | A/G | snv | 0.28 | 0.32 | 4 | |
| rs6668858 | 1 | 204166660 | intron variant | G/A | snv | 9.7E-03 | 4 | ||||
| rs734359 | 1 | 41480231 | intron variant | C/T | snv | 7.5E-02 | 4 | ||||
| rs10788994 | 1 | 55035303 | upstream gene variant | C/T | snv | 0.20 | 3 | ||||
| rs10858082 | 1 | 109256099 | intron variant | G/A | snv | 0.48 | 3 | ||||
| rs10888898 | 1 | 55050835 | intron variant | A/G | snv | 0.59 | 3 | ||||
| rs10889353 | 1 | 62652525 | intron variant | A/C;T | snv | 3 | |||||
| rs10916704 | 1 | 20074498 | intron variant | G/A;T | snv | 3 | |||||
| rs11206514 | 1 | 55050331 | intron variant | C/A | snv | 0.52 | 3 | ||||
| rs11573244 | 1 | 20081089 | intron variant | C/T | snv | 6.6E-03 | 3 | ||||
| rs11577931 | 1 | 109278262 | downstream gene variant | A/G | snv | 5.5E-02 | 3 | ||||
| rs1165287 | 1 | 55054539 | intron variant | G/A | snv | 0.52 | 3 | ||||
| rs11806129 | 1 | 94016821 | intron variant | A/G;T | snv | 3 | |||||
| rs11806638 | 1 | 55052487 | intron variant | C/A;G | snv | 3 | |||||
| rs12027135 | 1 | 25449242 | intron variant | A/T | snv | 0.50 | 3 | ||||
| rs12087003 | 1 | 94037627 | intron variant | A/G | snv | 6.3E-02 | 3 | ||||
| rs12097137 | 1 | 101243889 | downstream gene variant | G/A;T | snv | 3 | |||||
| rs12127701 | 1 | 109295642 | intron variant | A/G | snv | 6.2E-02 | 3 | ||||
| rs17035665 | 1 | 109271097 | intron variant | C/T | snv | 0.19 | 3 | ||||
| rs17111503 | 0.925 | 0.160 | 1 | 55037775 | upstream gene variant | A/G | snv | 0.22 | 3 | ||
| rs1748195 | 0.851 | 0.120 | 1 | 62583922 | intron variant | C/G;T | snv | 3 | |||
| rs17645031 | 1 | 109292316 | downstream gene variant | C/T | snv | 7.9E-02 | 3 | ||||
| rs17646665 | 1.000 | 0.080 | 1 | 109369429 | intron variant | A/G | snv | 5.8E-02 | 3 | ||
| rs17646731 | 1 | 109376903 | intron variant | G/A | snv | 4.6E-02 | 3 |