| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs74676849 | 1.000 | 0.040 | 7 | 11849866 | intergenic variant | A/G | snv | 2.6E-02 | 1 | ||
| rs755661906 | 1.000 | 0.040 | 10 | 90917732 | missense variant | C/T | snv | 1 | |||
| rs150793926 | 1.000 | 0.040 | 2 | 151924550 | intron variant | TA/-;TATA;TATATA | delins | 1 | |||
| rs143268013 | 1.000 | 0.040 | 9 | 100578527 | missense variant | C/G | snv | 1.2E-04 | 3.4E-04 | 1 | |
| rs751703046 | 1.000 | 0.040 | 9 | 100586276 | missense variant | G/C | snv | 9.9E-05 | 4.9E-05 | 1 | |
| rs137852764 | 1.000 | 0.040 | 11 | 19188211 | missense variant | T/C | snv | 2.0E-05 | 7.0E-06 | 1 | |
| rs767743962 | 1.000 | 0.040 | 2 | 219420290 | missense variant | C/A;T | snv | 4.0E-06; 8.0E-06 | 1 | ||
| rs1462311598 | 1.000 | 0.040 | X | 32390180 | missense variant | T/C | snv | 5.5E-06 | 1 | ||
| rs777064945 | 1.000 | 0.040 | 6 | 38722928 | missense variant | A/C;G | snv | 4.1E-06; 8.3E-06 | 1 | ||
| rs149399492 | 1.000 | 0.040 | 6 | 12292395 | missense variant | C/A;G;T | snv | 5.6E-05; 2.0E-05; 3.1E-04 | 1 | ||
| rs150035515 | 1.000 | 0.040 | 6 | 12292366 | synonymous variant | G/A;T | snv | 7.0E-04; 5.2E-05 | 1 | ||
| rs777846521 | 1.000 | 0.040 | 2 | 105386375 | missense variant | C/G;T | snv | 8.0E-06; 3.2E-05 | 1 | ||
| rs753641918 | 1.000 | 0.040 | 18 | 36755156 | missense variant | T/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs73920070 | 1.000 | 0.040 | 19 | 5851772 | intron variant | G/A | snv | 1.8E-02 | 1 | ||
| rs6660685 | 1.000 | 0.040 | 1 | 16020493 | intron variant | A/G | snv | 0.70 | 1 | ||
| rs7523558 | 1.000 | 0.040 | 1 | 16020237 | splice region variant | G/A | snv | 6.9E-02 | 1 | ||
| rs587777210 | 1.000 | 0.040 | X | 71305086 | missense variant | C/G | snv | 4.4E-05 | 2.8E-05 | 1 | |
| rs3740346 | 1.000 | 0.040 | 10 | 86692112 | intron variant | G/C | snv | 0.19 | 0.14 | 1 | |
| rs4468255 | 1.000 | 0.040 | 10 | 86679248 | intron variant | G/A;C | snv | 1 | |||
| rs56165849 | 1.000 | 0.040 | 10 | 86681952 | intron variant | A/G | snv | 0.50 | 1 | ||
| rs1165819867 | 1.000 | 0.040 | 1 | 156134892 | missense variant | G/A;T | snv | 1 | |||
| rs141490569 | 1.000 | 0.040 | 1 | 156136258 | missense variant | G/A | snv | 8.0E-05 | 9.8E-05 | 1 | |
| rs1553265180 | 1.000 | 0.040 | 1 | 156134500 | missense variant | T/A;G | snv | 1 | |||
| rs1553265739 | 1.000 | 0.040 | 1 | 156136081 | missense variant | A/T | snv | 1 | |||
| rs267607568 | 1.000 | 0.040 | 1 | 156115220 | missense variant | G/A;C;T | snv | 4.1E-06 | 1 |