| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4647924 | 0.600 | 0.520 | 4 | 1801844 | missense variant | C/A;G;T | snv | 4.2E-06; 4.2E-06 | 49 | ||
| rs1318358361 | 0.724 | 0.240 | 6 | 156778678 | missense variant | C/G | snv | 2.1E-05 | 13 | ||
| rs374608214 | 0.742 | 0.160 | 10 | 121520010 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 13 | |
| rs28931608 | 0.882 | 0.120 | 7 | 75985179 | missense variant | G/A;C | snv | 5.2E-05 | 3 | ||
| rs1554571213 | 0.925 | 0.080 | 8 | 96144601 | missense variant | A/T | snv | 2 | |||
| rs1211950654 | 1.000 | 0.080 | 2 | 72132463 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs148662051 | 1.000 | 0.080 | 15 | 98899591 | missense variant | G/A;T | snv | 3.2E-05; 4.0E-06 | 1 |