| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1021636 | 1.000 | 0.040 | 1 | 196876143 | intron variant | A/G | snv | 0.21 | 1 | ||
| rs10510109 | 1.000 | 0.040 | 10 | 122360941 | intergenic variant | G/A;T | snv | 1 | |||
| rs10754206 | 1.000 | 0.040 | 1 | 196851794 | intron variant | T/G | snv | 0.41 | 1 | ||
| rs10801575 | 1.000 | 0.040 | 1 | 196883651 | intron variant | T/A;C | snv | 1 | |||
| rs10887142 | 1.000 | 0.040 | 10 | 122347969 | downstream gene variant | G/A;C | snv | 1 | |||
| rs11200576 | 1.000 | 0.040 | 10 | 122358034 | intergenic variant | A/T | snv | 0.13 | 1 | ||
| rs11200583 | 1.000 | 0.040 | 10 | 122363954 | regulatory region variant | A/C | snv | 0.13 | 1 | ||
| rs12240143 | 1.000 | 0.040 | 1 | 196875887 | intron variant | T/C | snv | 0.39 | 1 | ||
| rs12240148 | 1.000 | 0.040 | 1 | 196876177 | intron variant | T/A;C | snv | 1 | |||
| rs1332666 | 1.000 | 0.040 | 1 | 197015549 | intergenic variant | A/G;T | snv | 1 | |||
| rs13374399 | 1.000 | 0.040 | 1 | 196872876 | intron variant | G/A | snv | 0.22 | 1 | ||
| rs13375144 | 1.000 | 0.040 | 1 | 196872560 | intron variant | C/T | snv | 0.22 | 1 | ||
| rs13375150 | 1.000 | 0.040 | 1 | 196872709 | intron variant | C/T | snv | 0.22 | 1 | ||
| rs13375236 | 1.000 | 0.040 | 1 | 196873141 | intron variant | C/T | snv | 0.22 | 1 | ||
| rs16840607 | 1.000 | 0.040 | 1 | 196853900 | intron variant | T/G | snv | 0.34 | 1 | ||
| rs16840639 | 0.925 | 0.120 | 1 | 196855643 | intron variant | T/C | snv | 0.23 | 1 | ||
| rs17050244 | 1.000 | 0.040 | 2 | 120525054 | regulatory region variant | A/C;G | snv | 1 | |||
| rs1738740 | 1.000 | 0.040 | 1 | 196839510 | intergenic variant | A/T | snv | 0.61 | 1 | ||
| rs17573790 | 1.000 | 0.040 | 1 | 196640266 | intergenic variant | A/C | snv | 6.9E-02 | 1 | ||
| rs1789110 | 0.925 | 0.040 | 18 | 77147088 | regulatory region variant | C/A | snv | 0.63 | 1 | ||
| rs2133138 | 1.000 | 0.040 | 1 | 196874041 | intron variant | G/A | snv | 0.22 | 1 | ||
| rs2336502 | 1.000 | 0.040 | 1 | 196873444 | intron variant | T/C | snv | 0.39 | 1 | ||
| rs2336503 | 1.000 | 0.040 | 1 | 196874290 | intron variant | C/A | snv | 0.22 | 1 | ||
| rs2842992 | 0.925 | 0.040 | 6 | 159650127 | intron variant | G/A | snv | 0.73 | 1 | ||
| rs3093077 | 0.827 | 0.200 | 1 | 159709846 | upstream gene variant | A/C;G;T | snv | 1 |