| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1127760 | 1.000 | 0.120 | 5 | 53484287 | missense variant | T/A | snv | 1 | |||
| rs1127761 | 1.000 | 0.120 | 5 | 53484289 | stop gained | T/A;C | snv | 2.8E-05 | 1 | ||
| rs11745088 | 1.000 | 0.120 | 5 | 53483680 | missense variant | G/C | snv | 4.4E-03 | 4.2E-03 | 1 | |
| rs1423560 | 1.000 | 0.120 | 5 | 53479932 | upstream gene variant | G/A;T | snv | 1 | |||
| rs3797297 | 1.000 | 0.120 | 5 | 53481826 | intron variant | G/T | snv | 0.18 | 1 | ||
| rs1159315 | 1.000 | 0.120 | 4 | 47001059 | intron variant | T/C | snv | 0.46 | 1 | ||
| rs10495960 | 1.000 | 0.120 | 2 | 48732893 | missense variant | G/A | snv | 0.18 | 0.14 | 1 | |
| rs7562215 | 1.000 | 0.120 | 2 | 48731548 | intron variant | G/A;T | snv | 1 | |||
| rs2272046 | 1.000 | 0.120 | 12 | 65830681 | intron variant | A/C | snv | 2.1E-02 | 1 | ||
| rs846908 | 1.000 | 0.120 | 1 | 209685108 | intron variant | A/G | snv | 0.97 | 1 | ||
| rs10459247 | 1.000 | 0.120 | 12 | 56777732 | intron variant | T/C | snv | 0.21 | 1 | ||
| rs10876920 | 1.000 | 0.120 | 12 | 56782391 | intron variant | C/G;T | snv | 0.50 | 1 | ||
| rs898611 | 1.000 | 0.120 | 12 | 56769532 | intron variant | C/G;T | snv | 1 | |||
| rs2060941 | 1.000 | 0.120 | 17 | 39826630 | intron variant | G/T | snv | 0.10 | 1 | ||
| rs9927163 | 1.000 | 0.120 | 16 | 3066185 | intron variant | T/A;G | snv | 1 | |||
| rs17253937 | 1.000 | 0.120 | 19 | 7184790 | intron variant | C/T | snv | 0.14 | 1 | ||
| rs2245648 | 1.000 | 0.120 | 19 | 7163219 | intron variant | T/C | snv | 0.22 | 0.27 | 1 | |
| rs2245649 | 1.000 | 0.120 | 19 | 7163203 | splice region variant | T/C | snv | 9.8E-02 | 0.13 | 1 | |
| rs2245655 | 1.000 | 0.120 | 19 | 7163129 | synonymous variant | T/G | snv | 9.8E-02 | 0.13 | 1 | |
| rs2962 | 1.000 | 0.120 | 19 | 7163054 | missense variant | G/A;T | snv | 6.4E-02 | 8.3E-02 | 1 | |
| rs3786681 | 1.000 | 0.120 | 19 | 7168922 | intron variant | A/G | snv | 0.24 | 1 | ||
| rs8107575 | 1.000 | 0.120 | 19 | 7165528 | intron variant | C/T | snv | 3.7E-02 | 1 | ||
| rs13164856 | 1.000 | 0.120 | 5 | 132477512 | intron variant | T/C | snv | 0.32 | 1 | ||
| rs2968909 | 1.000 | 0.120 | 12 | 2788698 | intron variant | C/G;T | snv | 1 | |||
| rs4409904 | 1.000 | 0.120 | 12 | 2776963 | intron variant | C/T | snv | 0.12 | 1 |