| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11066188 | 0.851 | 0.320 | 12 | 112172910 | intron variant | G/A;C | snv | 0.30; 4.1E-06 | 4 | ||
| rs11066301 | 0.827 | 0.200 | 12 | 112433568 | intron variant | A/G | snv | 0.30 | 4 | ||
| rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 8 | |||
| rs12035317 | 1.000 | 0.120 | 1 | 113553475 | intron variant | T/G | snv | 0.22 | 1 | ||
| rs4839335 | 1.000 | 0.120 | 1 | 113691249 | intergenic variant | G/A | snv | 0.74 | 1 | ||
| rs1111695 | 1.000 | 0.120 | 1 | 113701277 | intron variant | C/A | snv | 0.65 | 1 | ||
| rs1230647 | 1.000 | 0.120 | 1 | 113711017 | intron variant | C/T | snv | 0.78 | 1 | ||
| rs6679677 | 0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 | 6 | ||
| rs2797409 | 1.000 | 0.120 | 1 | 113787580 | intron variant | T/C | snv | 0.27 | 1 | ||
| rs1217413 | 1.000 | 0.120 | 1 | 113815128 | intron variant | G/A | snv | 0.82 | 1 | ||
| rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 | |
| rs1217407 | 1.000 | 0.120 | 1 | 113851126 | intron variant | A/G | snv | 0.77 | 1 | ||
| rs1217418 | 0.925 | 0.120 | 1 | 113858609 | intron variant | A/G | snv | 0.53 | 0.57 | 1 | |
| rs6665194 | 1.000 | 0.120 | 1 | 113875221 | intron variant | G/A;T | snv | 1 | |||
| rs12566340 | 0.925 | 0.200 | 1 | 113877706 | 3 prime UTR variant | C/A;T | snv | 1 | |||
| rs7529353 | 1.000 | 0.120 | 1 | 113877840 | 3 prime UTR variant | G/A | snv | 0.26 | 1 | ||
| rs7329468 | 1.000 | 0.120 | 13 | 113896878 | intron variant | C/G;T | snv | 0.23 | 1 | ||
| rs112630268 | 1.000 | 0.120 | 13 | 113919624 | non coding transcript exon variant | -/G | ins | 1 | |||
| rs9604529 | 1.000 | 0.120 | 13 | 113919624 | non coding transcript exon variant | A/G;T | snv | 0.17; 7.4E-06 | 1 | ||
| rs3810936 | 0.742 | 0.320 | 9 | 114790605 | synonymous variant | T/C | snv | 0.71 | 0.75 | 1 | |
| rs6478109 | 0.752 | 0.320 | 9 | 114806486 | upstream gene variant | A/G | snv | 0.74 | 2 | ||
| rs7848647 | 0.732 | 0.320 | 9 | 114806766 | upstream gene variant | T/C | snv | 0.74 | 1 | ||
| rs7940423 | 1.000 | 0.120 | 11 | 11482681 | intron variant | G/A | snv | 3.6E-02 | 1 | ||
| rs2736337 | 0.827 | 0.240 | 8 | 11484371 | upstream gene variant | T/C | snv | 0.26 | 2 | ||
| rs2736340 | 0.683 | 0.480 | 8 | 11486464 | upstream gene variant | C/T | snv | 0.25 | 7 |