| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs612169 | 9 | 133268030 | intron variant | G/A | snv | 10 | |||||
| rs630014 | 9 | 133274306 | intron variant | G/A;C | snv | 9 | |||||
| rs545971 | 9 | 133267960 | intron variant | T/A;C | snv | 8 | |||||
| rs643434 | 9 | 133266942 | intron variant | A/G;T | snv | 8 | |||||
| rs674302 | 9 | 133271249 | intron variant | A/T | snv | 8 | |||||
| rs644234 | 9 | 133266804 | intron variant | G/T | snv | 7 | |||||
| rs2066861 | 4 | 154606284 | intron variant | C/T | snv | 0.26 | 5 | ||||
| rs7681423 | 4 | 154621096 | intergenic variant | C/T | snv | 0.26 | 5 | ||||
| rs2420371 | 1 | 169522317 | intron variant | G/A | snv | 0.95 | 4 | ||||
| rs3758348 | 9 | 133372523 | intron variant | G/C | snv | 0.13 | 4 | ||||
| rs514708 | 9 | 133258352 | intron variant | C/T | snv | 0.29 | 4 | ||||
| rs626035 | 9 | 133259603 | intron variant | T/G | snv | 0.28 | 4 | ||||
| rs641943 | 9 | 133258323 | intron variant | A/G | snv | 0.29 | 4 | ||||
| rs641959 | 9 | 133258308 | intron variant | A/C | snv | 0.29 | 4 | ||||
| rs8176714 | 9 | 133257791 | intron variant | G/A | snv | 0.26 | 4 | ||||
| rs10886430 | 10 | 119250744 | intron variant | A/G | snv | 8.8E-02 | 3 | ||||
| rs12445050 | 16 | 81837364 | intron variant | C/T | snv | 9.6E-02 | 3 | ||||
| rs12644950 | 4 | 154616169 | upstream gene variant | G/A | snv | 0.25 | 3 | ||||
| rs1593 | 4 | 186274397 | 3 prime UTR variant | T/A;G | snv | 3 | |||||
| rs2073825 | 9 | 133257320 | intron variant | A/T | snv | 0.25 | 3 | ||||
| rs2073827 | 9 | 133261730 | intron variant | G/C | snv | 3 | |||||
| rs4253417 | 4 | 186277851 | intron variant | T/C;G | snv | 3 | |||||
| rs4524 | 1 | 169542517 | missense variant | T/C | snv | 0.28 | 0.24 | 3 | |||
| rs4805881 | 19 | 33405526 | intron variant | A/C | snv | 0.69 | 3 | ||||
| rs502361 | 9 | 133280016 | upstream gene variant | G/C | snv | 0.26 | 3 |