| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12210050 | 0.807 | 0.040 | 6 | 475489 | non coding transcript exon variant | C/T | snv | 0.11 | 4 | ||
| rs7297245 | 0.882 | 0.040 | 12 | 95980836 | missense variant | C/T | snv | 0.85 | 0.86 | 4 | |
| rs7335046 | 0.807 | 0.040 | 13 | 99389484 | downstream gene variant | G/C | snv | 0.80 | 4 | ||
| rs7309332 | 1.000 | 0.040 | 12 | 7938243 | upstream gene variant | T/C | snv | 0.59 | 3 | ||
| rs1047325 | 1.000 | 0.040 | 1 | 153561551 | missense variant | C/T | snv | 7.1E-02 | 0.16 | 2 | |
| rs10759637 | 1.000 | 0.040 | 9 | 113262744 | 3 prime UTR variant | A/C | snv | 0.47 | 2 | ||
| rs1670661 | 1.000 | 0.040 | 11 | 21209124 | intron variant | C/G;T | snv | 2 | |||
| rs1064793400 | 1.000 | 0.040 | 3 | 37048550 | missense variant | G/A | snv | 1 | |||
| rs1064793981 | 1.000 | 0.040 | 2 | 47475030 | missense variant | G/A | snv | 1 | |||
| rs1078305 | 1.000 | 0.040 | 9 | 121289122 | intron variant | A/G | snv | 0.70 | 1 | ||
| rs10818524 | 1.000 | 0.040 | 9 | 121267901 | intron variant | T/C | snv | 0.37 | 1 | ||
| rs10971638 | 1.000 | 0.040 | 9 | 33674679 | non coding transcript exon variant | C/T | snv | 0.21 | 1 | ||
| rs115169993 | 1.000 | 0.040 | 1 | 162772032 | missense variant | G/A | snv | 7.8E-04 | 2.9E-03 | 1 | |
| rs1295445617 | 1.000 | 0.040 | 2 | 47403398 | synonymous variant | G/A;C;T | snv | 4.5E-06; 4.5E-06 | 1 | ||
| rs1327891278 | 1.000 | 0.040 | 8 | 55950487 | missense variant | C/G | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs1607237 | 1.000 | 0.040 | 3 | 179232509 | intron variant | C/T | snv | 0.68 | 1 | ||
| rs2233914 | 1.000 | 0.040 | 9 | 113221260 | 5 prime UTR variant | G/A | snv | 0.16 | 0.13 | 1 | |
| rs2298211 | 1.000 | 0.040 | 1 | 1211863 | intron variant | A/C | snv | 8.1E-02 | 8.2E-02 | 1 | |
| rs3732183 | 1.000 | 0.040 | 2 | 47466820 | intron variant | G/A;T | snv | 0.34; 4.0E-06 | 0.40 | 1 | |
| rs454421 | 1.000 | 0.040 | 19 | 45341392 | intron variant | C/G;T | snv | 0.44 | 1 | ||
| rs45549733 | 1.000 | 0.040 | 11 | 67586503 | missense variant | C/G;T | snv | 7.6E-05 | 1 | ||
| rs470558 | 1.000 | 0.040 | 11 | 102795585 | synonymous variant | T/C | snv | 0.92 | 0.95 | 1 | |
| rs532172691 | 1.000 | 0.040 | 1 | 153563811 | stop gained | G/A | snv | 2.2E-04 | 3.4E-04 | 1 | |
| rs5854 | 1.000 | 0.040 | 11 | 102790143 | 3 prime UTR variant | G/A | snv | 0.29 | 1 | ||
| rs6413464 | 1.000 | 0.040 | 9 | 21970980 | missense variant | C/A;G | snv | 1.3E-03; 4.1E-06 | 1 |