| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs749547712 | 0.882 | 0.080 | 1 | 115768444 | missense variant | C/T | snv | 1.2E-05 | 3 | ||
| rs755492182 | 0.882 | 0.080 | 1 | 236735677 | missense variant | C/T | snv | 3 | |||
| rs1131820 | 0.925 | 0.080 | 1 | 154772376 | synonymous variant | A/G | snv | 0.77 | 0.71 | 2 | |
| rs12044963 | 1.000 | 0.080 | 1 | 111849738 | intron variant | G/T | snv | 0.10 | 2 | ||
| rs1296179669 | 0.925 | 0.160 | 1 | 11801338 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs13376333 | 0.925 | 0.080 | 1 | 154841877 | intron variant | C/T | snv | 0.28 | 2 | ||
| rs2660304 | 0.925 | 0.120 | 1 | 98046571 | non coding transcript exon variant | G/T | snv | 0.83 | 2 | ||
| rs2885697 | 1.000 | 0.080 | 1 | 41078607 | intron variant | G/T | snv | 0.72 | 2 | ||
| rs387906612 | 0.925 | 0.080 | 1 | 147759094 | stop gained | G/A | snv | 2 | |||
| rs61757261 | 0.925 | 0.080 | 1 | 11847373 | missense variant | T/G | snv | 2.0E-03 | 1.6E-03 | 2 | |
| rs6689306 | 0.925 | 0.080 | 1 | 154423470 | intron variant | A/G | snv | 0.61 | 2 | ||
| rs10753933 | 1.000 | 0.080 | 1 | 203057086 | intron variant | T/G | snv | 0.47 | 1 | ||
| rs10800507 | 1.000 | 0.080 | 1 | 170216500 | intron variant | C/G | snv | 0.47 | 1 | ||
| rs11264280 | 1.000 | 0.080 | 1 | 154890476 | intergenic variant | C/T | snv | 0.24 | 1 | ||
| rs11265611 | 1.000 | 0.080 | 1 | 154422649 | intron variant | G/A | snv | 0.59 | 1 | ||
| rs11579055 | 1.000 | 0.080 | 1 | 203062187 | intron variant | G/T | snv | 0.47 | 1 | ||
| rs11590635 | 1.000 | 0.080 | 1 | 48844092 | intron variant | G/A | snv | 1.6E-02 | 1 | ||
| rs12122060 | 1.000 | 0.080 | 1 | 170224718 | intron variant | T/A | snv | 7.9E-02 | 1 | ||
| rs12129500 | 1.000 | 0.080 | 1 | 154451288 | intron variant | T/C | snv | 0.60 | 1 | ||
| rs12142379 | 1.000 | 0.080 | 1 | 170724397 | intron variant | T/C | snv | 4.7E-02 | 1 | ||
| rs143945189 | 1.000 | 0.080 | 1 | 233666751 | missense variant | G/A;T | snv | 8.2E-03; 8.0E-06 | 1 | ||
| rs1443926 | 1.000 | 0.080 | 1 | 111919280 | intron variant | A/G | snv | 0.26 | 1 | ||
| rs146518726 | 1.000 | 0.080 | 1 | 51069367 | intergenic variant | G/A | snv | 1.8E-02 | 1 | ||
| rs1545300 | 1.000 | 0.080 | 1 | 111921382 | intron variant | C/T | snv | 0.25 | 1 | ||
| rs17375901 | 1.000 | 0.080 | 1 | 11792459 | intron variant | C/T | snv | 4.6E-02 | 1 |