| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2070016 | 1.000 | 0.040 | 4 | 154589162 | intron variant | A/G | snv | 0.12 | 3 | ||
| rs2073643 | 1.000 | 0.080 | 5 | 132387596 | intron variant | T/C | snv | 0.46 | 4 | ||
| rs2106854 | 5 | 132433482 | intron variant | C/T | snv | 0.23 | 3 | ||||
| rs2158177 | 0.925 | 0.120 | 5 | 132648366 | intron variant | A/G | snv | 0.18 | 4 | ||
| rs2227421 | 4 | 154571072 | 3 prime UTR variant | A/C | snv | 0.26 | 3 | ||||
| rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 5 | ||
| rs2286503 | 7 | 22816987 | intron variant | C/T | snv | 0.48 | 3 | ||||
| rs2522056 | 5 | 132466034 | intron variant | G/A | snv | 0.25 | 3 | ||||
| rs270607 | 5 | 132313493 | intron variant | A/G | snv | 0.69 | 3 | ||||
| rs3091307 | 0.925 | 0.160 | 5 | 132653444 | intron variant | A/G | snv | 0.34 | 3 | ||
| rs4129267 | 0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv | 5 | |||
| rs4220 | 0.925 | 0.080 | 4 | 154570607 | missense variant | G/A | snv | 0.17 | 0.15 | 3 | |
| rs434943 | 14 | 68847342 | intergenic variant | G/A | snv | 0.27 | 3 | ||||
| rs4463047 | 4 | 154574381 | downstream gene variant | T/C | snv | 0.15 | 3 | ||||
| rs4508864 | 4 | 154560137 | upstream gene variant | C/G;T | snv | 3 | |||||
| rs4537545 | 0.790 | 0.160 | 1 | 154446403 | intron variant | C/T | snv | 0.48 | 4 | ||
| rs4817986 | 21 | 39093586 | regulatory region variant | G/T | snv | 0.22 | 3 | ||||
| rs4925659 | 1 | 247440161 | intron variant | G/A | snv | 0.33 | 3 | ||||
| rs511154 | 3 | 136232079 | intergenic variant | A/G;T | snv | 3 | |||||
| rs6010044 | 22 | 50663510 | intergenic variant | A/C | snv | 0.20 | 3 | ||||
| rs6050 | 0.827 | 0.120 | 4 | 154586438 | missense variant | T/A;C | snv | 0.29 | 5 | ||
| rs6054 | 1.000 | 0.080 | 4 | 154568456 | missense variant | C/T | snv | 2.4E-03 | 2.7E-03 | 3 | |
| rs6056 | 4 | 154567669 | synonymous variant | C/T | snv | 0.17 | 0.15 | 3 | |||
| rs6058 | 4 | 154569192 | synonymous variant | G/T | snv | 5.2E-03 | 2.1E-02 | 3 | |||
| rs6734238 | 1.000 | 0.080 | 2 | 113083453 | upstream gene variant | A/G | snv | 0.39 | 4 |