| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1020731 | 1.000 | 0.080 | 2 | 160287544 | intron variant | G/A | snv | 0.69 | 1 | ||
| rs10195252 | 0.925 | 0.080 | 2 | 164656581 | intron variant | T/C | snv | 0.48 | 3 | ||
| rs1128249 | 1.000 | 0.080 | 2 | 164672114 | intron variant | G/C;T | snv | 1 | |||
| rs13389219 | 1.000 | 0.080 | 2 | 164672366 | intron variant | C/T | snv | 0.47 | 5 | ||
| rs7246865 | 19 | 17108295 | intron variant | G/A | snv | 0.36 | 1 | ||||
| rs9647379 | 3 | 172067378 | intron variant | G/C | snv | 0.32 | 1 | ||||
| rs1011731 | 1 | 172377408 | intron variant | G/A | snv | 0.46 | 1 | ||||
| rs6861681 | 5 | 173935455 | intron variant | G/A | snv | 0.22 | 1 | ||||
| rs12936587 | 0.882 | 0.080 | 17 | 17640408 | regulatory region variant | G/A | snv | 0.38 | 3 | ||
| rs3088050 | 5 | 177299634 | 3 prime UTR variant | G/A | snv | 0.18 | 1 | ||||
| rs543874 | 1.000 | 0.080 | 1 | 177920345 | upstream gene variant | A/G | snv | 0.21 | 2 | ||
| rs7637773 | 1.000 | 0.080 | 3 | 185797847 | intron variant | G/A | snv | 0.38 | 1 | ||
| rs7647305 | 1.000 | 0.080 | 3 | 186116501 | intron variant | T/C | snv | 0.74 | 3 | ||
| rs12061508 | 1.000 | 0.040 | 1 | 196615338 | intergenic variant | G/A | snv | 0.23 | 2 | ||
| rs505102 | 1 | 196650372 | upstream gene variant | T/C | snv | 0.40 | 1 | ||||
| rs15285 | 1.000 | 0.040 | 8 | 19967156 | 3 prime UTR variant | C/T | snv | 0.36 | 1 | ||
| rs2119690 | 8 | 20002028 | intergenic variant | G/A;C | snv | 1 | |||||
| rs12731740 | 1 | 207851475 | intron variant | C/T | snv | 9.1E-02 | 1 | ||||
| rs4640244 | 17 | 21380911 | intron variant | A/G | snv | 0.33 | 1 | ||||
| rs2820464 | 1 | 219519878 | intergenic variant | G/A;C | snv | 1 | |||||
| rs4846567 | 1 | 219577375 | regulatory region variant | G/T | snv | 0.23 | 1 | ||||
| rs2235529 | 1.000 | 0.040 | 1 | 22123994 | intron variant | C/T | snv | 0.13 | 1 | ||
| rs9750952 | 1.000 | 0.080 | 2 | 238827723 | intergenic variant | C/T | snv | 0.19 | 1 | ||
| rs1055144 | 1.000 | 0.040 | 7 | 25831489 | non coding transcript exon variant | C/T | snv | 0.16 | 2 | ||
| rs10019888 | 4 | 26061368 | regulatory region variant | A/G | snv | 0.17 | 2 |