| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12916300 | 0.742 | 0.080 | 15 | 28165345 | intron variant | C/T | snv | 0.50 | 13 | ||
| rs12913832 | 0.763 | 0.200 | 15 | 28120472 | intron variant | A/G | snv | 0.50 | 7 | ||
| rs1129038 | 0.851 | 0.120 | 15 | 28111713 | 3 prime UTR variant | C/T | snv | 0.49 | 0.50 | 6 | |
| rs1667394 | 15 | 28285036 | intron variant | C/A;T | snv | 3 | |||||
| rs1667392 | 15 | 28288419 | intron variant | G/A;C;T | snv | 2 | |||||
| rs8033755 | 1.000 | 0.080 | 15 | 28136400 | intron variant | C/A | snv | 0.84 | 1 | ||
| rs916977 | 1.000 | 0.080 | 15 | 28268218 | intron variant | T/C;G | snv | 1 | |||
| rs75165924 | 15 | 28135112 | intron variant | C/T | snv | 7.0E-02 | 1 | ||||
| rs79097182 | 15 | 28266851 | intron variant | C/T | snv | 6.1E-02 | 1 | ||||
| rs77572354 | 15 | 28315576 | intron variant | C/G;T | snv | 1 | |||||
| rs1635168 | 1.000 | 0.040 | 15 | 28290120 | intron variant | A/C | snv | 0.77 | 1 |