| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs1800896 | 0.507 | 0.800 | 1 | 206773552 | intron variant | T/C | snv | 0.41 | 113 | ||
| rs1137101 | 0.554 | 0.760 | 1 | 65592830 | missense variant | A/G | snv | 0.51 | 0.50 | 77 | |
| rs20417 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 57 | |||
| rs1061622 | 0.633 | 0.760 | 1 | 12192898 | missense variant | T/G | snv | 0.22 | 0.22 | 33 | |
| rs763110 | 0.653 | 0.560 | 1 | 172658358 | upstream gene variant | C/T | snv | 0.49 | 30 | ||
| rs1194611372 | 0.763 | 0.320 | 1 | 152032679 | missense variant | A/C | snv | 9 | |||
| rs1676486 | 0.851 | 0.120 | 1 | 102888582 | missense variant | A/G;T | snv | 0.80; 4.0E-06 | 7 | ||
| rs5030772 | 0.790 | 0.320 | 1 | 172664210 | intron variant | A/G | snv | 9.9E-02 | 7 | ||
| rs1034528 | 0.882 | 0.120 | 1 | 11189075 | intron variant | G/C | snv | 0.30 | 5 | ||
| rs2820436 | 0.882 | 0.040 | 1 | 219467338 | intergenic variant | A/C;G | snv | 4 | |||
| rs2615977 | 0.925 | 0.080 | 1 | 102986836 | intron variant | A/C | snv | 0.27 | 3 | ||
| rs2622873 | 0.882 | 0.040 | 1 | 103000497 | intron variant | T/C;G | snv | 3 | |||
| rs2785988 | 0.925 | 0.040 | 1 | 219570796 | intergenic variant | C/A | snv | 0.23 | 2 | ||
| rs3219463 | 0.925 | 0.120 | 1 | 45340760 | 5 prime UTR variant | C/T | snv | 0.27 | 2 | ||
| rs4233367 | 0.925 | 0.040 | 1 | 161193247 | missense variant | T/A;C | snv | 0.67 | 2 | ||
| rs4907986 | 0.925 | 0.040 | 1 | 103084077 | intron variant | C/T | snv | 0.49 | 2 | ||
| rs10218792 | 1.000 | 0.040 | 1 | 245587630 | intron variant | T/G | snv | 0.26 | 1 | ||
| rs11807350 | 1.000 | 0.040 | 1 | 161191145 | missense variant | C/T | snv | 3.1E-04 | 4.7E-04 | 1 | |
| rs1417066 | 1.000 | 0.040 | 1 | 219500486 | intergenic variant | G/A | snv | 0.43 | 1 | ||
| rs2353525 | 1.000 | 0.040 | 1 | 147597199 | intron variant | T/G | snv | 0.34 | 1 | ||
| rs41310883 | 1.000 | 0.040 | 1 | 151569700 | missense variant | C/G;T | snv | 8.0E-06; 1.2E-02 | 1 | ||
| rs4140564 | 1.000 | 0.040 | 1 | 186755871 | intergenic variant | G/A | snv | 0.93 | 1 | ||
| rs61735963 | 1.000 | 0.040 | 1 | 1341803 | missense variant | C/A;T | snv | 2.9E-05; 1.5E-02 | 1 | ||
| rs768876280 | 1.000 | 0.040 | 1 | 156881613 | missense variant | C/T | snv | 4.2E-06 | 2.1E-05 | 1 |