| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1273593548 | 0.716 | 0.160 | 7 | 106867593 | missense variant | T/G | snv | 8.4E-06 | 19 | ||
| rs1226994105 | 0.882 | 0.040 | 7 | 106868379 | missense variant | G/A | snv | 8.0E-06 | 5 | ||
| rs767132637 | 1.000 | 0.080 | 7 | 106867617 | missense variant | G/A | snv | 1.6E-05 | 3 | ||
| rs1129293 | 0.882 | 0.040 | 7 | 106872566 | synonymous variant | C/T | snv | 0.32 | 0.26 | 3 | |
| rs1412335442 | 0.925 | 0.120 | 7 | 106868317 | missense variant | G/T | snv | 7.0E-06 | 2 | ||
| rs2230460 | 0.925 | 0.040 | 7 | 106884244 | synonymous variant | C/T | snv | 0.12 | 8.5E-02 | 2 | |
| rs373644334 | 7 | 106867748 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06; 4.0E-06 | 1 | ||||
| rs1226137439 | 1.000 | 0.120 | 7 | 106868830 | synonymous variant | G/A | snv | 4.0E-06 | 1 | ||
| rs145459032 | 1.000 | 0.080 | 7 | 106867607 | missense variant | A/C;G | snv | 2.0E-05 | 2.1E-05 | 1 | |
| rs12536620 | 1.000 | 0.040 | 7 | 106904783 | intron variant | A/G | snv | 0.42 | 1 | ||
| rs12667819 | 1.000 | 0.040 | 7 | 106906212 | 3 prime UTR variant | G/A | snv | 0.41 | 1 | ||
| rs17847825 | 1.000 | 7 | 106868886 | missense variant | C/A;T | snv | 0.11 | 1 |