| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913355 | 0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 | 32 | ||
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 22 | ||
| rs121434596 | 0.677 | 0.440 | 1 | 114716123 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06 | 14 | ||
| rs121913364 | 0.641 | 0.520 | 7 | 140753334 | missense variant | T/C;G | snv | 4.0E-06 | 14 | ||
| rs121913369 | 0.790 | 0.280 | 7 | 140753346 | missense variant | G/A;C | snv | 4.0E-06 | 8 | ||
| rs121913315 | 0.882 | 0.160 | 19 | 1220488 | missense variant | G/A;T | snv | 5 | |||
| rs121913375 | 0.851 | 0.240 | 7 | 140753339 | missense variant | G/A;C | snv | 5 | |||
| rs121913341 | 0.851 | 0.280 | 7 | 140753350 | missense variant | A/C;T | snv | 3 | |||
| rs1057519730 | 1.000 | 0.040 | 15 | 66436786 | missense variant | T/A;G | snv | 2 | |||
| rs1057519837 | 1.000 | 0.040 | 3 | 41224631 | missense variant | C/G;T | snv | 2 | |||
| rs121913323 | 1.000 | 0.040 | 19 | 1220416 | stop gained | C/T | snv | 2 |