| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6873426 | 5 | 132482939 | 3 prime UTR variant | G/T | snv | 0.38 | 3 | ||||
| rs7896783 | 10 | 63402393 | intron variant | G/A;C | snv | 3 | |||||
| rs11242111 | 5 | 132420366 | intron variant | A/G;T | snv | 3 | |||||
| rs12777 | 5 | 132335969 | synonymous variant | C/G | snv | 3.1E-02 | 2.8E-02 | 3 | |||
| rs270607 | 5 | 132313493 | intron variant | A/G | snv | 0.69 | 3 | ||||
| rs7464572 | 8 | 143946999 | intron variant | C/A;G | snv | 3 | |||||
| rs10157379 | 1 | 247442297 | intron variant | C/G;T | snv | 3 | |||||
| rs1539019 | 0.882 | 0.240 | 1 | 247436999 | intron variant | A/C | snv | 0.63 | 3 | ||
| rs4925659 | 1 | 247440161 | intron variant | G/A | snv | 0.33 | 3 | ||||
| rs10512597 | 17 | 74703694 | intron variant | T/A;C | snv | 3 | |||||
| rs12915708 | 15 | 50756405 | intron variant | G/A;C | snv | 3 | |||||
| rs3091307 | 0.925 | 0.160 | 5 | 132653444 | intron variant | A/G | snv | 0.34 | 3 | ||
| rs2286503 | 7 | 22816987 | intron variant | C/T | snv | 0.48 | 3 |