| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
| rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
| rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 214 | |||
| rs878854066 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 213 | |||
| rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 188 | |
| rs1353702185 | 0.550 | 0.720 | 12 | 68839311 | missense variant | C/G | snv | 4.0E-06 | 79 | ||
| rs351855 | 0.597 | 0.560 | 5 | 177093242 | missense variant | G/A | snv | 0.33 | 0.26 | 58 | |
| rs1127354 | 0.667 | 0.400 | 20 | 3213196 | missense variant | C/A;G | snv | 7.5E-02 | 26 | ||
| rs12210538 | 1.000 | 0.040 | 6 | 110438805 | missense variant | A/G | snv | 0.17 | 0.16 | 3 | |
| rs10276036 | 1.000 | 0.040 | 7 | 87550882 | intron variant | C/A;T | snv | 1.2E-05; 0.53 | 1 | ||
| rs246221 | 1.000 | 0.040 | 16 | 16044465 | synonymous variant | T/C;G | snv | 0.33 | 1 | ||
| rs4148350 | 1.000 | 0.040 | 16 | 16076620 | intron variant | G/T | snv | 7.5E-02 | 1 | ||
| rs909530 | 1.000 | 0.040 | 1 | 171114034 | synonymous variant | C/T | snv | 0.29 | 0.32 | 1 |