| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2072660 | 1.000 | 0.080 | 1 | 154576245 | 3 prime UTR variant | T/C;G | snv | 1 | |||
| rs12466358 | 1.000 | 0.080 | 2 | 232532815 | intron variant | T/G | snv | 0.22 | 1 | ||
| rs1312171358 | 1.000 | 0.080 | 6 | 88144597 | synonymous variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs6928499 | 1.000 | 0.080 | 6 | 88151570 | intron variant | G/C | snv | 0.21 | 1 | ||
| rs879330 | 1.000 | 0.080 | 21 | 45408339 | intron variant | A/G | snv | 0.14 | 1 | ||
| rs2930357 | 1.000 | 0.080 | 8 | 3852138 | intron variant | T/C;G | snv | 1 | |||
| rs150922932 | 1.000 | 0.080 | 19 | 41094989 | missense variant | G/A | snv | 1.2E-05 | 4.9E-05 | 1 | |
| rs1438233520 | 1.000 | 0.080 | 19 | 40844742 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs780001693 | 1.000 | 0.080 | 19 | 40846921 | missense variant | T/C | snv | 2.0E-05 | 1 | ||
| rs45459594 | 1.000 | 0.080 | 19 | 41006966 | missense variant | C/G;T | snv | 8.0E-06; 1.3E-04 | 1 | ||
| rs1541333 | 1.000 | 0.080 | 9 | 133646263 | intron variant | C/G | snv | 0.52 | 1 | ||
| rs507506 | 1.000 | 0.080 | 17 | 7215003 | intron variant | A/G | snv | 0.55 | 1 | ||
| rs3003609 | 1.000 | 0.080 | 9 | 128222476 | synonymous variant | C/T | snv | 0.54 | 0.42 | 1 | |
| rs1334465665 | 1.000 | 0.080 | 11 | 113414400 | missense variant | C/T | snv | 2.1E-05 | 1 | ||
| rs4274224 | 1.000 | 0.080 | 11 | 113448730 | intron variant | G/A | snv | 0.49 | 1 | ||
| rs4648317 | 1.000 | 0.080 | 11 | 113460810 | intron variant | G/A | snv | 0.17 | 1 | ||
| rs16969868 | 1.000 | 0.080 | 13 | 107219364 | intron variant | G/C | snv | 3.8E-02 | 1 | ||
| rs2060762 | 1.000 | 0.080 | 7 | 50461686 | intron variant | A/G | snv | 0.81 | 1 | ||
| rs4424567 | 1.000 | 0.080 | 10 | 13759269 | 3 prime UTR variant | A/G | snv | 0.25 | 1 | ||
| rs222843 | 1.000 | 0.080 | 17 | 7242662 | non coding transcript exon variant | T/C | snv | 0.30 | 1 | ||
| rs2184026 | 1.000 | 0.080 | 9 | 98542066 | intron variant | C/G;T | snv | 0.25 | 1 | ||
| rs2491397 | 1.000 | 0.080 | 9 | 98442880 | intron variant | C/T | snv | 0.50 | 1 | ||
| rs2779562 | 1.000 | 0.080 | 9 | 98515399 | intron variant | T/C | snv | 0.48 | 1 | ||
| rs3750344 | 1.000 | 0.080 | 9 | 98578034 | synonymous variant | T/C | snv | 0.16 | 0.19 | 1 | |
| rs6570989 | 1.000 | 0.080 | 6 | 101509537 | intron variant | G/A | snv | 0.25 | 1 |