| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12634345 | 1.000 | 0.040 | 3 | 43097822 | intron variant | G/C | snv | 3.9E-02 | 1 | ||
| rs17470330 | 1.000 | 0.040 | 3 | 43098498 | intron variant | C/T | snv | 1.9E-02 | 1 | ||
| rs488069 | 0.925 | 0.080 | 3 | 43090952 | intron variant | C/T | snv | 0.79 | 1 | ||
| rs12497427 | 1.000 | 0.040 | 3 | 43083989 | intron variant | C/T | snv | 0.16 | 1 | ||
| rs493412 | 1.000 | 0.040 | 3 | 43084913 | intron variant | C/T | snv | 0.59 | 1 | ||
| rs11719573 | 1.000 | 0.040 | 3 | 43083698 | intron variant | C/T | snv | 0.17 | 1 | ||
| rs2867 | 1.000 | 0.040 | 3 | 43079343 | 3 prime UTR variant | T/G | snv | 0.11 | 1 | ||
| rs729654 | 3 | 43106160 | upstream gene variant | C/G;T | snv | 1 | |||||
| rs503100 | 1.000 | 0.040 | 3 | 43087416 | intron variant | A/T | snv | 0.95 | 1 | ||
| rs1523126 | 1.000 | 0.040 | 3 | 43090125 | intron variant | A/T | snv | 0.16 | 1 | ||
| rs7639740 | 1.000 | 0.040 | 3 | 43091527 | intron variant | C/A;T | snv | 1 | |||
| rs1815070 | 1.000 | 0.040 | 3 | 43092956 | intron variant | G/A;C | snv | 0.16 | 1 |