| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11448856 | 1.000 | 0.040 | 17 | 28357365 | frameshift variant | C/-;CC | delins | 6.2E-06; 1.00 | 1 | ||
| rs7854303 | 1.000 | 0.200 | 9 | 5557672 | missense variant | T/C | snv | 1.00 | 1.00 | 1 | |
| rs6264 | 0.925 | 0.040 | 7 | 50544037 | missense variant | T/C | snv | 1.00 | 0.99 | 2 | |
| rs25655 | 0.925 | 0.080 | 1 | 223712706 | missense variant | C/G | snv | 1.00 | 0.99 | 2 | |
| rs1169305 | 1.000 | 0.040 | 12 | 120999579 | missense variant | A/G | snv | 1.00 | 0.99 | 2 | |
| rs5348 | 1.000 | 0.080 | 13 | 77903539 | synonymous variant | A/G;T | snv | 1.00 | 1 | ||
| rs4879809 | 0.882 | 0.120 | 9 | 34635601 | 3 prime UTR variant | T/A;C;G | snv | 1.1E-03; 1.00 | 3 | ||
| rs616338 | 0.925 | 0.080 | 17 | 49219935 | missense variant | T/C | snv | 0.99 | 0.99 | 2 | |
| rs659497 | 1.000 | 0.120 | 17 | 42537437 | synonymous variant | T/C | snv | 0.99 | 0.99 | 1 | |
| rs155417 | 1.000 | 0.040 | 5 | 175441837 | synonymous variant | T/A;C | snv | 0.99 | 1 | ||
| rs868014 | 1.000 | 0.080 | 1 | 11789390 | missense variant | A/G | snv | 0.99 | 0.94 | 1 | |
| rs2251177 | 1.000 | 0.040 | 3 | 114139503 | missense variant | C/A;T | snv | 8.0E-06; 0.99 | 1 | ||
| rs1534284 | 0.925 | 0.040 | 12 | 53299748 | missense variant | A/G;T | snv | 0.99; 4.0E-06 | 2 | ||
| rs4804049 | 1.000 | 0.040 | 19 | 47320227 | synonymous variant | T/A;C | snv | 4.0E-06; 0.99 | 1 | ||
| rs4482737 | 1.000 | 0.040 | 4 | 47320173 | missense variant | T/C;G | snv | 0.99; 4.0E-06 | 2 | ||
| rs4844609 | 1.000 | 0.080 | 1 | 207609571 | missense variant | A/T | snv | 0.99 | 0.99 | 1 | |
| rs10282312 | 1.000 | 0.120 | 7 | 143320714 | missense variant | G/T | snv | 0.99 | 0.98 | 1 | |
| rs1801030 | 1.000 | 0.040 | 16 | 28606164 | missense variant | C/G;T | snv | 8.1E-06; 0.98 | 1 | ||
| rs1529927 | 1.000 | 0.040 | 16 | 56870675 | missense variant | C/G | snv | 1.6E-05; 0.98 | 0.98 | 1 | |
| rs5376 | 1.000 | 0.080 | 18 | 77268853 | missense variant | G/A | snv | 0.98 | 0.91 | 1 | |
| rs908832 | 0.851 | 0.120 | 9 | 137018032 | missense variant | A/C;G | snv | 0.97 | 0.96 | 4 | |
| rs3829462 | 1.000 | 0.040 | 15 | 58560880 | missense variant | C/A;T | snv | 0.97 | 1 | ||
| rs6472812 | 1.000 | 0.080 | 8 | 74004849 | missense variant | A/G | snv | 0.97 | 0.97 | 1 | |
| rs1146031 | 0.925 | 0.200 | 2 | 157770468 | synonymous variant | C/T | snv | 0.97 | 0.92 | 2 | |
| rs3211892 | 1.000 | 0.080 | 7 | 80661053 | intron variant | A/G | snv | 0.97 | 0.92 | 2 |