| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs397507525 | 0.925 | 0.160 | 12 | 112472968 | missense variant | C/T | snv | 7.0E-06 | 2 | ||
| rs765642157 | 1.000 | 0.160 | 12 | 112472969 | missense variant | T/A;G | snv | 4.0E-06 | 1 | ||
| rs397507526 | 1.000 | 0.160 | 12 | 112472972 | missense variant | T/A;G | snv | 1 | |||
| rs376607329 | 0.851 | 0.200 | 12 | 112472981 | missense variant | G/A;T | snv | 3.2E-05 | 3.5E-05 | 4 | |
| rs121918456 | 0.752 | 0.280 | 12 | 112473023 | missense variant | A/C;G | snv | 13 | |||
| rs397507529 | 0.851 | 0.160 | 12 | 112473031 | missense variant | A/G | snv | 7.0E-06 | 5 | ||
| rs397507531 | 0.752 | 0.320 | 12 | 112473040 | missense variant | T/C;G | snv | 18 | |||
| rs121918463 | 0.851 | 0.240 | 12 | 112477651 | missense variant | T/A;C;G | snv | 6 | |||
| rs28933386 | 0.752 | 0.400 | 12 | 112477719 | missense variant | A/G | snv | 1.2E-05 | 7.0E-06 | 15 | |
| rs121918455 | 0.695 | 0.440 | 12 | 112477720 | missense variant | A/C;G | snv | 31 | |||
| rs201787206 | 1.000 | 0.160 | 12 | 112477722 | missense variant | A/G | snv | 5.0E-04 | 2.5E-04 | 1 | |
| rs121918467 | 0.807 | 0.280 | 12 | 112486482 | missense variant | C/A;T | snv | 8.0E-06; 1.2E-05 | 23 | ||
| rs121918457 | 0.701 | 0.280 | 12 | 112488466 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 24 | |
| rs397507539 | 0.851 | 0.160 | 12 | 112489047 | missense variant | C/A;G;T | snv | 4.0E-06 | 8 | ||
| rs397507540 | 0.851 | 0.160 | 12 | 112489048 | missense variant | C/A;T | snv | 8 | |||
| rs397507541 | 0.827 | 0.160 | 12 | 112489068 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 5 | |
| rs397507542 | 0.790 | 0.320 | 12 | 112489069 | missense variant | G/T | snv | 9 | |||
| rs397507543 | 0.925 | 0.160 | 12 | 112489078 | missense variant | G/A | snv | 2 | |||
| rs121918458 | 0.807 | 0.320 | 12 | 112489080 | missense variant | T/A;G | snv | 8 | |||
| rs397507545 | 0.708 | 0.560 | 12 | 112489083 | missense variant | G/A;C | snv | 4.0E-06 | 20 | ||
| rs397507547 | 0.752 | 0.280 | 12 | 112489086 | missense variant | A/G | snv | 4.0E-06 | 14 | ||
| rs397507549 | 0.742 | 0.240 | 12 | 112489104 | missense variant | C/A;G | snv | 13 | |||
| rs121918470 | 0.790 | 0.160 | 12 | 112489105 | missense variant | A/C;G | snv | 4.0E-06 | 10 | ||
| rs397516797 | 1.000 | 0.160 | 12 | 112502222 | missense variant | C/T | snv | 4.0E-05 | 7.0E-05 | 1 | |
| rs267606920 | 0.882 | 0.160 | 1 | 114713911 | missense variant | C/T | snv | 7.0E-06 | 4 |