| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs63750215 | 0.701 | 0.240 | 1 | 226885603 | missense variant | A/T | snv | 19 | |||
| rs28936379 | 0.807 | 0.120 | 1 | 226888977 | missense variant | A/C;G;T | snv | 4.0E-06 | 10 | ||
| rs140501902 | 0.807 | 0.160 | 1 | 226883774 | missense variant | C/T | snv | 3.6E-03 | 3.4E-03 | 6 | |
| rs28936380 | 0.827 | 0.080 | 1 | 226885546 | missense variant | C/G;T | snv | 1.2E-05 | 5 | ||
| rs63749884 | 0.851 | 0.160 | 1 | 226888979 | missense variant | G/A | snv | 5 | |||
| rs58973334 | 0.882 | 0.080 | 1 | 226883748 | missense variant | G/A | snv | 8.6E-03 | 1.4E-02 | 3 | |
| rs61761208 | 0.882 | 0.080 | 1 | 226885602 | missense variant | A/T | snv | 3 | |||
| rs63750048 | 0.925 | 0.080 | 1 | 226883817 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs63750197 | 0.925 | 0.120 | 1 | 226885570 | missense variant | C/T | snv | 6.8E-04 | 7.2E-04 | 2 | |
| rs63750666 | 0.925 | 0.080 | 1 | 226895521 | missense variant | C/T | snv | 3.6E-05 | 2.1E-05 | 2 | |
| rs63750812 | 0.925 | 0.080 | 1 | 226885623 | missense variant | G/A | snv | 1.6E-05 | 1.4E-05 | 2 | |
| rs1553268799 | 1.000 | 0.080 | 1 | 226890135 | splice donor variant | TGA/- | del | 1 | |||
| rs63749851 | 1.000 | 0.080 | 1 | 226885545 | missense variant | A/C | snv | 1 |