| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1360590 | 1.000 | 0.040 | 9 | 22041444 | intron variant | T/C;G | snv | 2 | |||
| rs1537376 | 1.000 | 0.040 | 9 | 22116221 | intron variant | T/C | snv | 0.49 | 2 | ||
| rs1556515 | 1.000 | 0.040 | 9 | 22036368 | non coding transcript exon variant | C/T | snv | 0.71 | 2 | ||
| rs2069418 | 1.000 | 0.040 | 9 | 22009699 | intron variant | G/C | snv | 0.70 | 2 | ||
| rs2106119 | 1.000 | 0.040 | 9 | 22017551 | intron variant | A/G;T | snv | 2 | |||
| rs2106120 | 1.000 | 0.040 | 9 | 22017102 | intron variant | G/T | snv | 0.56 | 2 | ||
| 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 | |||
| 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 | ||
| 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 | ||
| rs1532085 | 0.882 | 0.080 | 15 | 58391167 | intron variant | A/G;T | snv | 13 | |||
| rs1412834 | 0.790 | 0.080 | 9 | 22110132 | intron variant | T/C | snv | 0.64 | 11 | ||
| rs173539 | 0.882 | 0.080 | 16 | 56954132 | intergenic variant | C/T | snv | 0.33 | 11 | ||
| rs12678919 | 0.882 | 0.080 | 8 | 19986711 | intergenic variant | A/G | snv | 1.0E-01 | 10 | ||
| rs445925 | 0.882 | 0.080 | 19 | 44912383 | non coding transcript exon variant | G/A;C | snv | 10 |