| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3772622 | 0.851 | 0.080 | 3 | 148717966 | intron variant | T/A;C | snv | 4 | |||
| rs1492100 | 1.000 | 0.040 | 3 | 148719640 | intron variant | T/A | snv | 0.34 | 1 | ||
| rs5182 | 0.742 | 0.160 | 3 | 148741608 | synonymous variant | C/T | snv | 0.49 | 0.41 | 16 | |
| rs5186 | 0.630 | 0.560 | 3 | 148742201 | 3 prime UTR variant | A/C | snv | 0.23 | 0.21 | 38 | |
| rs71413689 | 1.000 | 0.040 | 2 | 150398953 | intergenic variant | G/A | snv | 1.7E-02 | 1 | ||
| rs13361189 | 0.752 | 0.240 | 5 | 150843825 | upstream gene variant | T/C | snv | 0.21 | 13 | ||
| rs4958847 | 0.807 | 0.120 | 5 | 150860025 | intron variant | G/A | snv | 0.25 | 8 | ||
| rs1057156731 | 0.925 | 0.120 | 1 | 156137730 | missense variant | T/A | snv | 3 | |||
| rs4880 | 0.500 | 0.840 | 6 | 159692840 | missense variant | A/G | snv | 0.48 | 0.47 | 131 | |
| rs1130864 | 0.672 | 0.520 | 1 | 159713301 | 3 prime UTR variant | G/A | snv | 0.26 | 27 | ||
| rs117542855 | 1.000 | 0.040 | 11 | 1635713 | regulatory region variant | C/G;T | snv | 3.1E-02 | 1 | ||
| rs2710833 | 0.925 | 0.080 | 4 | 168488807 | intron variant | T/A;C | snv | 2 | |||
| rs5854292 | 0.851 | 0.080 | 3 | 168680960 | intron variant | AA/-;A;AAA | delins | 5 | |||
| rs5748926 | 1.000 | 0.040 | 22 | 17168884 | upstream gene variant | T/C | snv | 0.70 | 1 | ||
| rs1131580 | 0.882 | 0.160 | 3 | 172505830 | 3 prime UTR variant | A/C;G;T | snv | 4 | |||
| rs7946 | 0.851 | 0.160 | 17 | 17506246 | missense variant | C/T | snv | 0.59 | 0.59 | 6 | |
| rs13306741 | 1.000 | 0.040 | 17 | 17811708 | 3 prime UTR variant | C/A;T | snv | 4.3E-03; 7.4E-06 | 1 | ||
| rs11868035 | 0.763 | 0.200 | 17 | 17811787 | splice region variant | G/A | snv | 0.45 | 0.33 | 14 | |
| rs1292932521 | 1.000 | 0.040 | 22 | 18517476 | missense variant | C/T | snv | 1 | |||
| rs4686434 | 1.000 | 0.040 | 3 | 186647354 | intron variant | A/C;G | snv | 1 | |||
| rs266729 | 0.637 | 0.560 | 3 | 186841685 | upstream gene variant | C/A;G;T | snv | 37 | |||
| rs822393 | 0.882 | 0.160 | 3 | 186848537 | intron variant | C/T | snv | 0.30 | 3 | ||
| rs2241766 | 0.608 | 0.720 | 3 | 186853103 | synonymous variant | T/C;G | snv | 8.0E-06; 0.13 | 48 | ||
| rs1501299 | 0.597 | 0.720 | 3 | 186853334 | intron variant | G/C;T | snv | 52 | |||
| rs2241767 | 0.763 | 0.440 | 3 | 186853407 | intron variant | A/G | snv | 0.10 | 10 |