| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4755453 | 0.925 | 0.080 | 11 | 36509094 | intron variant | C/A;G;T | snv | 2 | |||
| rs352162 | 0.882 | 0.160 | 3 | 52218953 | non coding transcript exon variant | T/C | snv | 0.55 | 3 | ||
| rs7022797 | 0.882 | 0.120 | 9 | 88989548 | upstream gene variant | T/G | snv | 0.38 | 3 | ||
| rs1475145065 | 0.882 | 0.080 | 14 | 24574706 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 3 | ||
| rs2839693 | 0.882 | 0.120 | 10 | 44379119 | intron variant | T/A;C | snv | 3 | |||
| rs805305 | 0.882 | 0.120 | 6 | 31729610 | intron variant | C/G | snv | 0.48 | 3 | ||
| rs773520745 | 0.882 | 0.120 | 19 | 18075817 | missense variant | C/G;T | snv | 2.0E-05; 4.0E-06 | 3 | ||
| rs374520012 | 0.882 | 0.120 | 20 | 38373994 | missense variant | T/C;G | snv | 8.0E-06; 4.0E-06 | 3 | ||
| rs1764390 | 0.882 | 0.160 | 1 | 34794360 | missense variant | A/C;G;T | snv | 0.61 | 0.69 | 3 | |
| rs10506481 | 0.882 | 0.080 | 12 | 66250331 | 3 prime UTR variant | T/C | snv | 9.0E-02 | 3 | ||
| rs12048215 | 0.882 | 0.160 | 1 | 247421289 | intron variant | A/G | snv | 0.11 | 3 | ||
| rs2027432 | 0.882 | 0.160 | 1 | 247415139 | upstream gene variant | A/G;T | snv | 3 | |||
| rs6958571 | 0.925 | 0.080 | 7 | 30446094 | intron variant | A/C;G | snv | 1.2E-05; 0.25; 5.3E-05 | 3 | ||
| rs2664581 | 0.882 | 0.120 | 20 | 45175881 | missense variant | A/C | snv | 0.16 | 0.16 | 3 | |
| rs17036188 | 0.882 | 0.120 | 3 | 12299426 | intron variant | T/C | snv | 4.0E-02 | 3 | ||
| rs2972164 | 0.925 | 0.080 | 3 | 12292917 | intron variant | T/C | snv | 0.46 | 3 | ||
| rs4684846 | 0.882 | 0.080 | 3 | 12297350 | intron variant | A/G | snv | 0.28 | 3 | ||
| rs7119750 | 0.882 | 0.120 | 11 | 65655120 | 3 prime UTR variant | C/G;T | snv | 3 | |||
| rs11137480 | 0.882 | 0.120 | 9 | 88989662 | upstream gene variant | G/C | snv | 0.37 | 3 | ||
| rs773829498 | 0.882 | 0.080 | 7 | 101130457 | missense variant | A/G | snv | 4.0E-06 | 3 | ||
| rs77874543 | 0.882 | 0.080 | 22 | 41926712 | missense variant | G/C;T | snv | 6.1E-02 | 5.5E-02 | 3 | |
| rs5743867 | 0.882 | 0.120 | 11 | 1307121 | intron variant | G/A;C | snv | 3 | |||
| rs1524668 | 0.851 | 0.160 | 2 | 9557243 | upstream gene variant | A/C | snv | 0.64 | 4 | ||
| rs2721068 | 0.882 | 0.160 | 13 | 40565575 | intron variant | T/C | snv | 0.38 | 4 | ||
| rs368287711 | 0.851 | 0.120 | 11 | 117989554 | missense variant | C/A;T | snv | 2.0E-05; 2.4E-05 | 4 |