| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs672607 | 0.851 | 0.040 | 1 | 147581540 | intron variant | G/A | snv | 0.12 | 4 | ||
| rs688325 | 0.851 | 0.040 | 1 | 147605490 | intron variant | G/A | snv | 0.19 | 4 | ||
| rs72737330 | 0.925 | 0.080 | 1 | 216600151 | intron variant | T/C | snv | 0.15 | 4 | ||
| rs111365677 | 0.925 | 0.040 | 1 | 99463578 | upstream gene variant | T/C | snv | 2.3E-03 | 3 | ||
| rs12128108 | 0.925 | 0.040 | 1 | 49827749 | intron variant | C/G;T | snv | 3 | |||
| rs1541187 | 0.882 | 0.040 | 1 | 147579693 | intron variant | C/G;T | snv | 3 | |||
| rs159963 | 1.000 | 0.040 | 1 | 8444361 | intron variant | C/A | snv | 0.52 | 3 | ||
| rs1620977 | 1.000 | 0.040 | 1 | 72263459 | intron variant | A/G;T | snv | 3 | |||
| rs1935881 | 0.882 | 0.080 | 1 | 190097256 | downstream gene variant | T/C | snv | 0.28 | 3 | ||
| rs2984618 | 0.925 | 0.040 | 1 | 47224766 | intron variant | G/T | snv | 0.52 | 3 | ||
| rs4839421 | 0.925 | 0.040 | 1 | 110479338 | intron variant | C/A | snv | 0.40 | 3 | ||
| rs55679149 | 0.925 | 0.040 | 1 | 89068655 | upstream gene variant | C/T | snv | 0.34 | 3 | ||
| rs7555693 | 0.925 | 0.040 | 1 | 106295917 | intergenic variant | G/A | snv | 0.45 | 3 | ||
| rs760161369 | 0.882 | 0.040 | 1 | 11800214 | missense variant | G/A;C | snv | 2.8E-05; 4.0E-06 | 3 | ||
| rs946903 | 0.882 | 0.040 | 1 | 147625465 | 3 prime UTR variant | T/C | snv | 0.25 | 3 | ||
| rs10789340 | 0.925 | 0.120 | 1 | 72474590 | intron variant | A/G;T | snv | 2 | |||
| rs10914456 | 1.000 | 0.040 | 1 | 31622570 | intron variant | T/C | snv | 0.51 | 2 | ||
| rs11209175 | 1.000 | 0.040 | 1 | 67909145 | intron variant | C/T | snv | 0.54 | 2 | ||
| rs11209948 | 1.000 | 0.040 | 1 | 72346221 | intron variant | G/C;T | snv | 2 | |||
| rs116362708 | 1.000 | 0.040 | 1 | 75464629 | intron variant | G/A | snv | 2.3E-02 | 2 | ||
| rs12030991 | 1.000 | 0.040 | 1 | 106683737 | intergenic variant | G/C;T | snv | 2 | |||
| rs12036147 | 1.000 | 0.040 | 1 | 239835413 | intron variant | A/G;T | snv | 2 | |||
| rs12068879 | 1.000 | 0.040 | 1 | 14959860 | intron variant | A/G | snv | 0.18 | 2 | ||
| rs12129573 | 0.925 | 0.040 | 1 | 73302683 | upstream gene variant | C/A | snv | 0.31 | 2 | ||
| rs12137398 | 1.000 | 0.040 | 1 | 7730488 | intron variant | C/T | snv | 0.14 | 2 |