Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs261332 | 0.851 | 0.120 | 15 | 58435126 | non coding transcript exon variant | A/G | snv | 0.80 | 17 | ||
| rs1532085 | 0.882 | 0.080 | 15 | 58391167 | intron variant | A/G;T | snv | 7 | |||
| rs2070895 | 0.807 | 0.120 | 15 | 58431740 | intron variant | G/A | snv | 0.33 | 7 | ||
| rs10468017 | 0.851 | 0.120 | 15 | 58386313 | intron variant | C/T | snv | 0.24 | 6 | ||
| rs2043085 | 0.827 | 0.080 | 15 | 58388755 | intron variant | T/C | snv | 0.54 | 6 | ||
| rs2043082 | 15 | 58382109 | intron variant | G/A | snv | 0.32 | 4 | ||||
| rs261291 | 1.000 | 0.080 | 15 | 58387979 | intron variant | T/A;C | snv | 4 | |||
| rs4775041 | 1.000 | 0.040 | 15 | 58382496 | intron variant | G/C | snv | 0.24 | 4 | ||
| rs1077834 | 15 | 58431280 | intron variant | T/C | snv | 0.34 | 4 | ||||
| rs13329672 | 15 | 58407738 | intron variant | C/T | snv | 0.31 | 3 | ||||
| rs1601935 | 15 | 58379566 | intron variant | G/T | snv | 0.60 | 3 | ||||
| rs7350789 | 15 | 58387469 | intron variant | G/A | snv | 0.35 | 3 | ||||
| rs1077835 | 15 | 58431227 | intron variant | A/G | snv | 0.34 | 3 | ||||
| rs1800588 | 0.790 | 0.200 | 15 | 58431476 | intron variant | C/G;T | snv | 0.30 | 3 | ||
| rs261342 | 15 | 58438954 | intron variant | G/A;C;T | snv | 3 | |||||
| rs261334 | 15 | 58434545 | intron variant | G/C | snv | 0.73 | 3 | ||||
| rs588136 | 15 | 58438299 | intron variant | C/G;T | snv | 2 | |||||
| rs8034802 | 15 | 58432593 | intron variant | T/A | snv | 0.33 | 1 | ||||
| rs261336 | 15 | 58450219 | intron variant | G/A | snv | 0.81 | 1 |