| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3091367 | 1.000 | 0.080 | 22 | 37831814 | 3 prime UTR variant | C/G | snv | 0.27 | 1 | ||
| rs6486120 | 1.000 | 0.080 | 11 | 13302595 | intron variant | T/G | snv | 0.57 | 1 | ||
| rs2832387 | 1.000 | 0.080 | 21 | 29518574 | intron variant | A/G | snv | 0.54 | 1 | ||
| rs4923463 | 1.000 | 0.080 | 11 | 27650953 | intron variant | A/G | snv | 0.17 | 1 | ||
| rs10913569 | 1.000 | 0.080 | 1 | 178548873 | non coding transcript exon variant | A/G;T | snv | 1 | |||
| rs25917 | 1.000 | 0.080 | 5 | 111473151 | intron variant | A/G | snv | 0.11 | 1 | ||
| rs2239670 | 1.000 | 0.080 | 5 | 71719676 | non coding transcript exon variant | A/G;T | snv | 1 | |||
| rs615470 | 1.000 | 0.080 | 15 | 78593646 | 3 prime UTR variant | T/C | snv | 0.64 | 1 | ||
| rs910924 | 1.000 | 0.080 | 17 | 752680 | 5 prime UTR variant | G/A | snv | 0.20 | 1 | ||
| rs1116313 | 1.000 | 0.080 | 11 | 113425385 | intron variant | A/G | snv | 0.45 | 1 | ||
| rs2734835 | 1.000 | 0.080 | 11 | 113420621 | intron variant | T/G | snv | 0.43 | 1 | ||
| rs10892169 | 1.000 | 0.080 | 11 | 117762339 | intron variant | A/G | snv | 0.68 | 1 | ||
| rs780312650 | 1.000 | 0.080 | 11 | 1558231 | missense variant | G/A | snv | 8.0E-06 | 1 | ||
| rs12597786 | 1.000 | 0.080 | 16 | 53787395 | intron variant | C/T | snv | 3.2E-02 | 1 | ||
| rs8062891 | 1.000 | 0.080 | 16 | 54055160 | intron variant | T/C | snv | 0.80 | 1 | ||
| rs29220 | 1.000 | 0.080 | 6 | 29621889 | intron variant | C/G | snv | 0.31 | 1 | ||
| rs172677 | 1.000 | 0.080 | 12 | 13944536 | intron variant | A/G | snv | 0.63 | 1 | ||
| rs34315573 | 1.000 | 0.080 | 12 | 13866194 | synonymous variant | C/T | snv | 4.9E-02 | 3.4E-02 | 1 | |
| rs886003 | 1.000 | 0.080 | 7 | 127206962 | intron variant | C/T | snv | 0.15 | 1 | ||
| rs17862325 | 1.000 | 0.080 | 7 | 127214599 | intron variant | A/G | snv | 0.21 | 1 | ||
| rs6060124 | 1.000 | 0.080 | 20 | 34949094 | intron variant | C/A | snv | 0.27 | 1 | ||
| rs10160548 | 1.000 | 0.080 | 11 | 113985959 | intron variant | G/T | snv | 0.54 | 1 | ||
| rs33940208 | 1.000 | 0.080 | 11 | 113975355 | synonymous variant | C/T | snv | 8.2E-02 | 7.0E-02 | 1 | |
| rs2276305 | 1.000 | 0.080 | 11 | 113932382 | synonymous variant | G/A;C;T | snv | 7.7E-02; 2.8E-03; 5.2E-05 | 1 | ||
| rs1057302 | 1.000 | 0.080 | 1 | 175157287 | 3 prime UTR variant | A/G | snv | 0.38 | 1 |