| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1501299 | 0.597 | 0.720 | 3 | 186853334 | intron variant | G/C;T | snv | 52 | |||
| rs2241766 | 0.608 | 0.720 | 3 | 186853103 | synonymous variant | T/C;G | snv | 8.0E-06; 0.13 | 48 | ||
| rs1049353 | 0.630 | 0.600 | 6 | 88143916 | synonymous variant | C/T | snv | 0.21 | 0.20 | 42 | |
| rs266729 | 0.637 | 0.560 | 3 | 186841685 | upstream gene variant | C/A;G;T | snv | 37 | |||
| rs17855750 | 0.695 | 0.480 | 16 | 28503907 | missense variant | A/C;T | snv | 6.4E-02; 4.0E-06 | 21 | ||
| rs822396 | 0.732 | 0.400 | 3 | 186849088 | intron variant | G/A | snv | 0.81 | 16 | ||
| rs185847354 | 0.763 | 0.160 | 3 | 186854460 | missense variant | T/C | snv | 3.1E-04 | 7.0E-05 | 11 | |
| rs3865188 | 0.790 | 0.320 | 16 | 82617112 | intergenic variant | A/G;T | snv | 10 | |||
| rs26528 | 0.807 | 0.200 | 16 | 28506388 | intron variant | T/C | snv | 0.43 | 9 | ||
| rs17366743 | 0.807 | 0.280 | 3 | 186854300 | missense variant | T/C | snv | 2.2E-02 | 2.1E-02 | 7 | |
| rs40837 | 0.925 | 0.120 | 16 | 28499524 | 3 prime UTR variant | A/G | snv | 0.43 | 5 | ||
| rs1656930 | 1.000 | 0.080 | 3 | 186835068 | intergenic variant | A/G | snv | 0.86 | 3 | ||
| rs822393 | 0.882 | 0.160 | 3 | 186848537 | intron variant | C/T | snv | 0.30 | 3 | ||
| rs62625753 | 0.925 | 0.120 | 3 | 186854237 | missense variant | G/A | snv | 3.0E-03 | 2.9E-03 | 3 | |
| rs121917815 | 0.925 | 0.120 | 3 | 186854303 | missense variant | C/T | snv | 4.0E-06; 1.2E-05 | 3 | ||
| rs199646033 | 0.925 | 0.120 | 3 | 186854219 | stop gained | G/A;T | snv | 4.4E-05; 4.0E-06 | 3 | ||
| rs950561906 | 0.925 | 0.120 | 12 | 113398775 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 3 |