| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs780881510 | 0.925 | 0.080 | 17 | 39715299 | missense variant | A/C | snv | 1.2E-05 | 2 | ||
| rs1801201 | 1.000 | 0.080 | 17 | 39723332 | missense variant | A/C;G | snv | 4.0E-06; 4.9E-03 | 1 | ||
| rs759478535 | 0.851 | 0.080 | 17 | 39708351 | missense variant | A/G | snv | 6.8E-05 | 4.2E-05 | 6 | |
| rs1485579458 | 0.851 | 0.080 | 17 | 39723921 | missense variant | A/G | snv | 4.0E-06 | 4 | ||
| rs1396809633 | 0.925 | 0.080 | 17 | 39711979 | missense variant | A/G | snv | 7.0E-06 | 2 | ||
| rs1136201 | 0.645 | 0.280 | 17 | 39723335 | missense variant | A/G;T | snv | 0.20 | 33 | ||
| rs1801200 | 0.790 | 0.200 | 17 | 39723335 | missense variant | A/G;T | snv | 7 | |||
| rs977818812 | 1.000 | 0.040 | 17 | 39723608 | missense variant | A/T | snv | 3 | |||
| rs1057519816 | 0.763 | 0.200 | 17 | 39711955 | missense variant | C/A;T | snv | 6 | |||
| rs747200104 | 0.925 | 0.080 | 17 | 39717388 | missense variant | C/A;T | snv | 8.0E-06 | 2 | ||
| rs757811990 | 0.925 | 0.080 | 17 | 39710413 | missense variant | C/A;T | snv | 4.0E-06 | 2 | ||
| rs1058808 | 0.658 | 0.360 | 17 | 39727784 | missense variant | C/G | snv | 0.61 | 0.52 | 27 | |
| rs61552325 | 0.882 | 0.080 | 17 | 39727784 | missense variant | C/G | snv | 5 | |||
| rs1324255598 | 1.000 | 0.080 | 17 | 39725780 | missense variant | C/G | snv | 4.0E-06 | 1 | ||
| rs758222990 | 1.000 | 0.080 | 17 | 39725363 | missense variant | C/G;T | snv | 1.2E-05 | 1 | ||
| rs752295912 | 0.925 | 0.080 | 17 | 39710398 | missense variant | C/T | snv | 1.6E-05 | 6 | ||
| rs767151455 | 0.925 | 0.080 | 17 | 39708379 | missense variant | C/T | snv | 8.0E-06 | 4 | ||
| rs1416532705 | 0.882 | 0.080 | 17 | 39709435 | missense variant | C/T | snv | 4.0E-06 | 3 | ||
| rs751074421 | 0.925 | 0.080 | 17 | 39715823 | missense variant | C/T | snv | 8.0E-06 | 3 | ||
| rs778798172 | 0.925 | 0.080 | 17 | 39723321 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs372811772 | 17 | 39708435 | synonymous variant | C/T | snv | 8.0E-06 | 2.1E-05 | 2 | |||
| rs2517951 | 0.925 | 0.080 | 17 | 39696844 | intron variant | C/T | snv | 0.52 | 2 | ||
| rs2643194 | 0.925 | 0.080 | 17 | 39696795 | 5 prime UTR variant | C/T | snv | 0.67 | 2 | ||
| rs527779103 | 0.925 | 0.080 | 17 | 39708528 | missense variant | C/T | snv | 5.4E-04 | 1.4E-04 | 2 | |
| rs542027040 | 17 | 39724864 | missense variant | C/T | snv | 1.2E-05 | 1 |