| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1052571 | 0.882 | 0.080 | 1 | 15524118 | missense variant | G/A | snv | 0.50 | 0.59 | 4 | |
| rs77485247 | 0.925 | 0.080 | 18 | 24460578 | upstream gene variant | T/A | snv | 3 | |||
| rs426496 | 1.000 | 0.040 | 12 | 49954295 | synonymous variant | T/C | snv | 0.77 | 0.71 | 3 | |
| rs3840634 | 0.925 | 0.120 | 7 | 116556798 | intron variant | T/C | snv | 2 | |||
| rs3736309 | 0.925 | 0.120 | 12 | 49964271 | intron variant | A/G | snv | 0.12 | 2 | ||
| rs1274867386 | 1.000 | 0.040 | 10 | 123150118 | missense variant | T/A | snv | 7.0E-06 | 1 | ||
| rs2234688 | 1.000 | 0.040 | 12 | 68158742 | intron variant | -/G;TGAG;TGG;TGTGG;TGTGTGAG;TGTGTGG;TGTGTGTGG | delins | 1 | |||
| rs17173510 | 1.000 | 0.040 | 21 | 34449551 | synonymous variant | C/G;T | snv | 4.0E-06; 3.6E-03 | 6.6E-03 | 1 | |
| rs3746951 | 1.000 | 0.040 | 21 | 43426136 | missense variant | C/A;T | snv | 0.23 | 1 | ||
| rs3087969 | 1.000 | 0.040 | 19 | 10627963 | missense variant | C/G;T | snv | 4.0E-06; 0.79 | 1 | ||
| rs487119 | 1.000 | 0.040 | 2 | 40261737 | intron variant | G/A | snv | 0.54 | 1 |