| 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 | |||||
| rs75885714 | 3 | 16901018 | intron variant | A/C | snv | 4.6E-02 | 7 | ||||
| rs2169387 | 8 | 9323885 | intron variant | A/G | snv | 0.87 | 6 | ||||
| rs2731672 | 5 | 177415473 | intron variant | T/C | snv | 0.66 | 6 | ||||
| rs77303550 | 16 | 72045758 | intron variant | C/T | snv | 0.19 | 6 | ||||
| rs16850073 | 4 | 73838282 | 3 prime UTR variant | C/T | snv | 0.29 | 5 | ||||
| rs2280401 | 19 | 49496752 | intron variant | G/A | snv | 0.12 | 5 | ||||
| rs10211524 | 2 | 64980940 | intron variant | G/A | snv | 0.51 | 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 | ||||
| rs10265221 | 7 | 151717243 | intron variant | T/A;C | snv | 3 | |||||
| rs10466351 | 11 | 92964815 | upstream gene variant | C/T | snv | 0.48 | 3 | ||||
| rs12741825 | 1 | 159700355 | downstream gene variant | C/T | snv | 0.24 | 3 | ||||
| rs14399 | 6 | 111222741 | 3 prime UTR variant | C/A | snv | 0.32 | 3 | ||||
| rs2040771 | 22 | 19174422 | downstream gene variant | C/A;T | snv | 3 | |||||
| rs2073825 | 9 | 133257320 | intron variant | A/T | snv | 0.25 | 3 | ||||
| rs517414 | 9 | 133258643 | intron variant | G/A | snv | 0.26 | 3 |