| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10189857 | 1.000 | 0.080 | 2 | 60486100 | intron variant | A/G | snv | 0.42 | 5 | ||
| rs16978075 | 18 | 44533186 | intron variant | T/C | snv | 8.5E-02 | 5 | ||||
| rs6704768 | 1.000 | 0.040 | 2 | 232727791 | intron variant | G/A | snv | 0.54 | 4 | ||
| rs71636784 | 1.000 | 0.040 | 1 | 26842709 | intron variant | T/G | snv | 0.12 | 4 | ||
| rs7832708 | 8 | 10332530 | intron variant | C/T | snv | 0.49 | 4 | ||||
| rs9388490 | 1.000 | 0.080 | 6 | 126383649 | intron variant | C/T | snv | 0.42 | 4 | ||
| rs10752262 | 1.000 | 0.040 | 10 | 12353101 | intron variant | C/T | snv | 0.39 | 3 | ||
| rs11765189 | 1.000 | 0.040 | 7 | 157743285 | intron variant | A/G | snv | 0.25 | 3 | ||
| rs12602286 | 1.000 | 0.040 | 17 | 19333641 | intron variant | G/T | snv | 0.79 | 3 | ||
| rs13262595 | 1.000 | 0.040 | 8 | 142235609 | intron variant | A/C;G | snv | 3 | |||
| rs2093210 | 1.000 | 0.040 | 14 | 60490561 | intron variant | C/T | snv | 0.45 | 3 | ||
| rs2629540 | 0.925 | 0.080 | 10 | 124737579 | intron variant | G/C | snv | 0.18 | 3 | ||
| rs2764261 | 6 | 108606639 | intron variant | A/G;T | snv | 3 | |||||
| rs4396807 | 22 | 37742372 | intron variant | G/C | snv | 0.38 | 3 | ||||
| rs6119267 | 20 | 32576112 | intron variant | C/A;G | snv | 3 | |||||
| rs613872 | 0.851 | 0.120 | 18 | 55543071 | intron variant | G/T | snv | 0.88 | 3 | ||
| rs62154720 | 1.000 | 0.040 | 2 | 105306623 | intron variant | C/T | snv | 9.2E-02 | 3 | ||
| rs6870983 | 5 | 88401716 | intron variant | C/T | snv | 0.29 | 3 | ||||
| rs72829446 | 17 | 7648805 | intron variant | C/T | snv | 6.5E-02 | 3 | ||||
| rs75757892 | 6 | 7232156 | intron variant | C/T | snv | 0.12 | 3 | ||||
| rs76076331 | 1.000 | 0.040 | 2 | 10837459 | intron variant | C/T | snv | 1.0E-01 | 3 | ||
| rs7963801 | 12 | 79291446 | intron variant | T/C | snv | 0.70 | 3 | ||||
| rs9616914 | 1.000 | 0.040 | 22 | 50678709 | intron variant | G/A | snv | 0.35 | 0.36 | 3 | |
| rs10949662 | 7 | 157741413 | intron variant | C/A;T | snv | 2 | |||||
| rs10954772 | 8 | 31006422 | intron variant | T/A;C | snv | 2 |