| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2184061 | 1.000 | 0.040 | 9 | 22061563 | intron variant | C/A;T | snv | 0.64 | 2 | ||
| rs4977575 | 1.000 | 0.040 | 9 | 22124745 | intron variant | C/G;T | snv | 2 | |||
| rs4977753 | 1.000 | 0.040 | 9 | 22030028 | non coding transcript exon variant | C/T | snv | 0.58 | 2 | ||
| rs543830 | 1.000 | 0.040 | 9 | 22026640 | intron variant | A/C;T | snv | 2 | |||
| rs6475608 | 1.000 | 0.080 | 9 | 22101703 | intron variant | T/C | snv | 0.60 | 2 | ||
| rs679038 | 1.000 | 0.040 | 9 | 22029081 | intron variant | G/A;T | snv | 2 | |||
| rs7027048 | 1.000 | 0.040 | 9 | 22053710 | intron variant | A/G;T | snv | 2 | |||
| rs7027950 | 1.000 | 0.040 | 9 | 22048392 | intron variant | C/T | snv | 0.49 | 2 | ||
| rs7028268 | 1.000 | 0.040 | 9 | 22048415 | intron variant | G/A | snv | 0.32 | 2 | ||
| rs7028570 | 1.000 | 0.040 | 9 | 22048684 | intron variant | G/A | snv | 0.50 | 2 | ||
| rs7030641 | 1.000 | 0.040 | 9 | 22054041 | intron variant | C/T | snv | 0.72 | 2 | ||
| rs7341786 | 9 | 22112242 | intron variant | A/C | snv | 0.65 | 2 | ||||
| rs7859362 | 9 | 22105928 | intron variant | T/C | snv | 0.64 | 2 | ||||
| rs7866783 | 1.000 | 0.040 | 9 | 22056360 | non coding transcript exon variant | A/G | snv | 0.71 | 2 | ||
| rs8181050 | 1.000 | 0.040 | 9 | 22064392 | intron variant | G/A;C;T | snv | 2 | |||
| rs944799 | 1.000 | 0.040 | 9 | 22050614 | intron variant | A/G | snv | 0.50 | 2 | ||
| rs9632885 | 1.000 | 0.040 | 9 | 22072639 | intron variant | G/A | snv | 0.56 | 2 | ||
| rs2069418 | 1.000 | 0.040 | 9 | 22009699 | intron variant | G/C | snv | 0.70 | 2 | ||
| rs3809346 | 1.000 | 0.080 | 13 | 110308596 | intron variant | G/A;C | snv | 2 | |||
| rs3798722 | 6 | 11040190 | intron variant | A/G | snv | 0.39 | 2 | ||||
| rs448792 | 1.000 | 0.080 | 13 | 32103287 | intron variant | T/A;C | snv | 2 | |||
| rs543554 | 1.000 | 0.080 | 13 | 32127501 | intron variant | A/G;T | snv | 2 | |||
| rs6606859 | 1.000 | 0.080 | 15 | 27032254 | intron variant | C/A;T | snv | 2 | |||
| rs9973676 | 1.000 | 0.080 | 2 | 230954091 | intron variant | G/A | snv | 5.8E-02 | 2 | ||
| rs8134546 | 1.000 | 0.080 | 21 | 34782568 | intron variant | T/C | snv | 8.7E-02 | 2 |