| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4650608 | 0.851 | 0.040 | 1 | 78772330 | intergenic variant | T/C | snv | 0.29 | 7 | ||
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 6 | |
| rs2252865 | 0.851 | 0.040 | 1 | 8362616 | intron variant | T/C | snv | 0.72 | 6 | ||
| rs1625579 | 0.763 | 0.160 | 1 | 98037378 | intron variant | G/T | snv | 0.78 | 5 | ||
| rs6694545 | 0.851 | 0.040 | 1 | 29964421 | intergenic variant | A/G | snv | 0.58 | 5 | ||
| rs6586354 | 0.851 | 0.040 | 1 | 234897489 | intron variant | G/A | snv | 0.25 | 4 | ||
| rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 4 | |
| rs115777110 | 0.882 | 0.040 | 1 | 208936211 | intergenic variant | T/C | snv | 1.2E-02 | 3 | ||
| rs146330533 | 0.882 | 0.040 | 1 | 17669971 | intron variant | G/A | snv | 1.2E-02 | 3 | ||
| rs6703335 | 0.882 | 0.040 | 1 | 243445665 | intron variant | A/G | snv | 0.50 | 3 | ||
| rs10489744 | 0.925 | 0.040 | 1 | 165411386 | intron variant | G/A | snv | 0.55 | 2 | ||
| rs11162556 | 0.925 | 0.040 | 1 | 78795698 | intergenic variant | A/G | snv | 0.32 | 2 | ||
| rs150404479 | 1.000 | 0.040 | 1 | 43222879 | missense variant | T/C | snv | 9.1E-03 | 9.8E-03 | 2 | |
| rs16836940 | 0.925 | 0.040 | 1 | 150444437 | intron variant | A/G | snv | 0.31 | 2 | ||
| rs17018311 | 1.000 | 0.040 | 1 | 211981666 | intron variant | T/C | snv | 2.7E-02 | 2 | ||
| rs10489167 | 1.000 | 0.040 | 1 | 40710794 | intron variant | G/A | snv | 0.13 | 1 | ||
| rs10889182 | 1.000 | 0.040 | 1 | 60532523 | intron variant | T/G | snv | 0.33 | 1 | ||
| rs10889187 | 1.000 | 0.040 | 1 | 60545086 | intron variant | G/A | snv | 0.33 | 1 | ||
| rs10889189 | 1.000 | 0.040 | 1 | 60559354 | intron variant | C/G | snv | 0.47 | 1 | ||
| rs11207633 | 1.000 | 0.040 | 1 | 60541510 | non coding transcript exon variant | A/G | snv | 0.32 | 1 | ||
| rs1125777 | 1.000 | 0.040 | 1 | 61366218 | intron variant | C/T | snv | 0.42 | 1 | ||
| rs12144699 | 1.000 | 0.040 | 1 | 59139525 | intron variant | G/A | snv | 2.3E-02 | 1 | ||
| rs12563333 | 1.000 | 0.040 | 1 | 220484892 | downstream gene variant | C/T | snv | 3.7E-02 | 1 | ||
| rs12568010 | 1.000 | 0.040 | 1 | 61366266 | intron variant | A/G | snv | 9.8E-02 | 1 | ||
| rs17121983 | 1.000 | 0.040 | 1 | 61354400 | intron variant | C/G;T | snv | 1 |