| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4072037 | 0.732 | 0.240 | 1 | 155192276 | splice acceptor variant | C/A;T | snv | 0.59 | 22 | ||
| rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 22 | ||
| rs4245739 | 0.708 | 0.360 | 1 | 204549714 | 3 prime UTR variant | C/A;G | snv | 0.77; 6.2E-06 | 21 | ||
| rs5068 | 0.776 | 0.160 | 1 | 11845917 | 3 prime UTR variant | A/G;T | snv | 13 | |||
| rs3753584 | 0.827 | 0.080 | 1 | 11804529 | 5 prime UTR variant | T/C | snv | 0.14 | 10 | ||
| rs17367504 | 1.000 | 0.040 | 1 | 11802721 | intron variant | A/G | snv | 0.14 | 9 | ||
| rs880315 | 0.925 | 0.120 | 1 | 10736809 | intron variant | T/C | snv | 0.32 | 9 | ||
| rs17030613 | 1 | 112648185 | intron variant | A/C | snv | 0.19 | 7 | ||||
| rs34517439 | 0.882 | 0.120 | 1 | 77984833 | intron variant | C/A | snv | 7.3E-02 | 7 | ||
| rs17035646 | 1 | 10736490 | intron variant | G/A;T | snv | 6 | |||||
| rs2004776 | 1 | 230712956 | intron variant | C/G;T | snv | 5 | |||||
| rs3790604 | 1 | 112504257 | intron variant | C/A | snv | 7.8E-02 | 5 | ||||
| rs4660293 | 1 | 39562508 | non coding transcript exon variant | A/C;G | snv | 5 | |||||
| rs10776752 | 1 | 112501706 | intron variant | G/T | snv | 8.8E-02 | 4 | ||||
| rs12129649 | 1 | 112688881 | 5 prime UTR variant | G/T | snv | 6.6E-02 | 4 | ||||
| rs2493134 | 1 | 230713613 | intron variant | T/C | snv | 0.57 | 4 | ||||
| rs2932538 | 1 | 112673921 | intron variant | A/C;G | snv | 4 | |||||
| rs2999159 | 1 | 112688136 | intron variant | A/G | snv | 0.85 | 4 | ||||
| rs34071855 | 1 | 10738432 | intron variant | C/G;T | snv | 4 | |||||
| rs72640287 | 1 | 11905735 | upstream gene variant | C/T | snv | 2.6E-02 | 4 | ||||
| rs10745332 | 1 | 112646431 | intron variant | G/A | snv | 0.77 | 3 | ||||
| rs12046278 | 1 | 10739520 | intron variant | T/C | snv | 0.36 | 3 | ||||
| rs12063100 | 1 | 188865413 | downstream gene variant | G/A;T | snv | 3 | |||||
| rs12118370 | 1 | 112605645 | intron variant | A/G | snv | 0.24 | 3 | ||||
| rs1330225 | 1 | 106293321 | intergenic variant | T/C | snv | 0.38 | 3 |