| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13334632 | 1.000 | 0.080 | 16 | 87457213 | intron variant | T/C | snv | 0.16 | 1 | ||
| rs1334465665 | 1.000 | 0.080 | 11 | 113414400 | missense variant | C/T | snv | 2.1E-05 | 1 | ||
| rs1411836 | 1.000 | 0.080 | 9 | 89160966 | intron variant | C/G;T | snv | 0.12 | 1 | ||
| rs1438233520 | 1.000 | 0.080 | 19 | 40844742 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs1465781973 | 1.000 | 0.080 | 11 | 113395026 | missense variant | C/T | snv | 2.0E-05 | 1 | ||
| rs147586937 | 1.000 | 0.080 | 15 | 78602096 | synonymous variant | G/A | snv | 4.8E-05 | 2.8E-05 | 1 | |
| rs150922932 | 1.000 | 0.080 | 19 | 41094989 | missense variant | G/A | snv | 1.2E-05 | 4.9E-05 | 1 | |
| rs1541333 | 1.000 | 0.080 | 9 | 133646263 | intron variant | C/G | snv | 0.52 | 1 | ||
| rs1547696 | 1.000 | 0.080 | 9 | 89079205 | intron variant | T/C | snv | 0.60 | 1 | ||
| rs1556384 | 1.000 | 0.080 | 9 | 89149212 | intron variant | T/C | snv | 0.93 | 1 | ||
| rs1659400 | 1.000 | 0.080 | 9 | 84711079 | intron variant | A/G | snv | 0.60 | 1 | ||
| rs16969868 | 1.000 | 0.080 | 13 | 107219364 | intron variant | G/C | snv | 3.8E-02 | 1 | ||
| rs17710 | 1.000 | 0.080 | 17 | 7240675 | 3 prime UTR variant | A/T | snv | 0.10 | 1 | ||
| rs2060762 | 1.000 | 0.080 | 7 | 50461686 | intron variant | A/G | snv | 0.81 | 1 | ||
| rs2072660 | 1.000 | 0.080 | 1 | 154576245 | 3 prime UTR variant | T/C;G | snv | 1 | |||
| rs2184026 | 1.000 | 0.080 | 9 | 98542066 | intron variant | C/G;T | snv | 0.25 | 1 | ||
| rs222843 | 1.000 | 0.080 | 17 | 7242662 | non coding transcript exon variant | T/C | snv | 0.30 | 1 | ||
| rs2236196 | 1.000 | 0.080 | 20 | 63346204 | 3 prime UTR variant | G/A;C | snv | 0.71 | 1 | ||
| rs2241617 | 1.000 | 0.080 | 16 | 87407442 | 3 prime UTR variant | T/C | snv | 0.11 | 1 | ||
| rs2273504 | 1.000 | 0.080 | 20 | 63356709 | intron variant | G/A;T | snv | 1 | |||
| rs2273505 | 1.000 | 0.080 | 20 | 63359526 | non coding transcript exon variant | C/T | snv | 4.0E-06; 9.2E-02 | 9.5E-02 | 1 | |
| rs2297313 | 1.000 | 0.080 | 9 | 89054447 | intron variant | A/G | snv | 0.41 | 1 | ||
| rs2302762 | 1.000 | 0.080 | 17 | 7455542 | non coding transcript exon variant | T/C | snv | 0.61 | 1 | ||
| rs2302763 | 1.000 | 0.080 | 17 | 7455958 | intron variant | T/C;G | snv | 0.18 | 1 | ||
| rs2302765 | 1.000 | 0.080 | 17 | 7447656 | splice region variant | T/C | snv | 0.18 | 0.17 | 1 |