Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1800588 | 0.790 | 0.200 | 15 | 58431476 | intron variant | C/G;T | snv | 0.30 | 6 | ||
| rs261332 | 0.851 | 0.120 | 15 | 58435126 | non coding transcript exon variant | A/G | snv | 0.80 | 6 | ||
| rs8033940 | 15 | 58432643 | intron variant | G/A | snv | 0.41 | 5 | ||||
| rs8034802 | 15 | 58432593 | intron variant | T/A | snv | 0.33 | 5 | ||||
| rs261336 | 15 | 58450219 | intron variant | G/A | snv | 0.81 | 5 | ||||
| rs588136 | 15 | 58438299 | intron variant | C/G;T | snv | 5 | |||||
| rs473224 | 15 | 58445142 | intron variant | T/A;G | snv | 5 | |||||
| rs261342 | 15 | 58438954 | intron variant | G/A;C;T | snv | 5 | |||||
| rs2070895 | 0.807 | 0.120 | 15 | 58431740 | intron variant | G/A | snv | 0.33 | 5 | ||
| rs485538 | 15 | 58448978 | intron variant | C/G;T | snv | 5 | |||||
| rs485671 | 15 | 58448935 | intron variant | A/C;T | snv | 5 | |||||
| rs261338 | 15 | 58442806 | intron variant | A/G | snv | 0.83 | 5 | ||||
| rs1077835 | 15 | 58431227 | intron variant | A/G | snv | 0.34 | 3 | ||||
| rs10518982 | 15 | 58507555 | intron variant | A/G | snv | 2.2E-02 | 3 | ||||
| rs16940391 | 15 | 58507449 | intron variant | C/A;G | snv | 3 | |||||
| rs261334 | 15 | 58434545 | intron variant | G/C | snv | 0.73 | 3 | ||||
| rs10518983 | 15 | 58520578 | intron variant | C/T | snv | 5.4E-02 | 1 | ||||
| rs12324244 | 15 | 58520749 | intron variant | C/G;T | snv | 1 | |||||
| rs1077834 | 15 | 58431280 | intron variant | T/C | snv | 0.34 | 1 |