| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs706778 | 0.695 | 0.320 | 10 | 6056986 | intron variant | C/T | snv | 0.46 | 15 | ||
| rs61839660 | 0.776 | 0.280 | 10 | 6052734 | intron variant | C/T | snv | 5.7E-02 | 9 | ||
| rs2104286 | 0.662 | 0.440 | 10 | 6057082 | intron variant | T/C | snv | 0.18 | 7 | ||
| rs7909519 | 0.807 | 0.120 | 10 | 6047878 | intron variant | T/G | snv | 7.2E-02 | 6 | ||
| rs2476491 | 0.776 | 0.240 | 10 | 6053447 | intron variant | A/T | snv | 0.25 | 6 | ||
| rs3118471 | 0.827 | 0.120 | 10 | 6060794 | intron variant | A/G | snv | 0.24 | 5 | ||
| rs12722486 | 1.000 | 10 | 6061799 | intron variant | C/A;T | snv | 5 | ||||
| rs12722502 | 0.882 | 0.080 | 10 | 6051176 | intron variant | C/T | snv | 7.8E-03 | 4 | ||
| rs706779 | 0.827 | 0.160 | 10 | 6056861 | intron variant | T/C | snv | 0.48 | 4 | ||
| rs3118470 | 0.752 | 0.360 | 10 | 6059750 | intron variant | T/A;C | snv | 2 | |||
| rs12722489 | 0.882 | 0.160 | 10 | 6060049 | intron variant | C/T | snv | 0.11 | 2 | ||
| rs12722515 | 1.000 | 0.040 | 10 | 6039267 | intron variant | C/A | snv | 0.13 | 2 | ||
| rs1107345 | 0.925 | 0.160 | 10 | 6045332 | intron variant | G/T | snv | 0.18 | 2 | ||
| rs9663421 | 1.000 | 0.080 | 10 | 6013641 | intron variant | C/A;T | snv | 1 | |||
| rs12722495 | 0.851 | 0.200 | 10 | 6055320 | intron variant | T/C | snv | 7.0E-02 | 1 | ||
| rs7893467 | 1.000 | 0.040 | 10 | 6037072 | intron variant | G/C;T | snv | 1 | |||
| rs3118469 | 10 | 6059166 | intron variant | A/T | snv | 0.24 | 1 | ||||
| rs12722561 | 1.000 | 0.080 | 10 | 6027930 | intron variant | C/A;T | snv | 1 | |||
| rs12253981 | 1.000 | 0.080 | 10 | 6050383 | intron variant | T/G | snv | 0.29 | 1 | ||
| rs12722547 | 10 | 6030130 | intron variant | G/C | snv | 7.8E-03 | 1 | ||||
| rs7090504 | 10 | 6049054 | intron variant | T/A | snv | 0.16 | 1 | ||||
| rs4747846 | 10 | 6032488 | intron variant | G/A;C;T | snv | 1 |