| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1482518887 | 0.790 | 0.040 | 21 | 34887018 | missense variant | C/T | snv | 7.0E-06 | 8 | ||
| rs11079041 | 0.882 | 0.040 | 17 | 42262061 | intron variant | T/A;C | snv | 0.36 | 4 | ||
| rs1188975135 | 0.882 | 0.040 | 22 | 39017772 | missense variant | T/C | snv | 4.0E-06 | 4 | ||
| rs138817062 | 0.882 | 0.040 | 15 | 74044940 | missense variant | C/T | snv | 4.0E-05 | 7.0E-06 | 4 | |
| rs35602083 | 0.851 | 0.040 | 13 | 28049450 | missense variant | C/T | snv | 1.7E-02 | 1.6E-02 | 4 | |
| rs139834892 | 0.882 | 0.040 | 19 | 43553481 | missense variant | C/T | snv | 6.4E-05 | 1.1E-04 | 3 | |
| rs2308950 | 0.882 | 0.040 | 1 | 15507011 | missense variant | C/G;T | snv | 4.0E-06; 1.1E-02 | 3 | ||
| rs6964823 | 0.925 | 0.040 | 7 | 50392398 | intron variant | G/A | snv | 0.45 | 3 | ||
| rs766274360 | 0.882 | 0.040 | 16 | 2713697 | missense variant | G/T | snv | 1.2E-05 | 3 | ||
| rs10931910 | 0.925 | 0.040 | 2 | 200659013 | intron variant | A/G;T | snv | 2 | |||
| rs1258094111 | 0.925 | 0.040 | 14 | 24575388 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs17886724 | 0.925 | 0.040 | 17 | 42344145 | intron variant | A/G | snv | 0.35 | 2 | ||
| rs201045130 | 0.925 | 0.040 | 1 | 39659467 | missense variant | A/G | snv | 9.9E-05 | 1.0E-04 | 2 | |
| rs201820837 | 0.925 | 0.040 | 12 | 11869532 | missense variant | G/A;T | snv | 2.4E-05; 6.4E-05 | 2 | ||
| rs587782006 | 0.925 | 0.040 | 17 | 7673761 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs754894156 | 0.925 | 0.040 | 21 | 34834544 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs765669662 | 0.925 | 0.040 | 8 | 85465317 | missense variant | G/A;T | snv | 2.0E-05; 4.0E-06 | 2 | ||
| rs947141826 | 0.925 | 0.040 | 10 | 133394281 | missense variant | C/T | snv | 2.1E-05 | 2 | ||
| rs10065633 | 1.000 | 0.040 | 5 | 132481024 | intron variant | T/C | snv | 0.38 | 1 | ||
| rs113017087 | 1.000 | 0.040 | 5 | 112737780 | intron variant | T/C | snv | 5.4E-03 | 1 | ||
| rs115658307 | 1.000 | 0.040 | 5 | 112707537 | 5 prime UTR variant | C/T | snv | 4.8E-03 | 1 | ||
| rs138386816 | 1.000 | 0.040 | 5 | 112707566 | 5 prime UTR variant | C/T | snv | 7.2E-03 | 1 | ||
| rs1416364034 | 1.000 | 0.040 | 17 | 42300731 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs1444068378 | 1.000 | 0.040 | 2 | 105363404 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs6413463 | 1.000 | 0.040 | 9 | 21970990 | missense variant | A/G;T | snv | 2.9E-05; 3.0E-04 | 1 |