| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs892295 | 3 | 355870 | intron variant | A/G | snv | 0.87 | 4 | ||||
| rs2078087 | 1 | 183389270 | intron variant | C/T | snv | 0.16 | 4 | ||||
| rs12483959 | 1.000 | 22 | 43930116 | intron variant | G/A;C;T | snv | 4 | ||||
| rs13077101 | 3 | 120706484 | intron variant | T/C | snv | 4 | |||||
| rs10001545 | 4 | 87254878 | intergenic variant | C/A;T | snv | 3 | |||||
| rs10883437 | 1.000 | 0.040 | 10 | 100035604 | regulatory region variant | T/A;G | snv | 0.43 | 3 | ||
| rs144104656 | 1.000 | 0.120 | 2 | 118661291 | regulatory region variant | A/G | snv | 1.1E-03 | 3 | ||
| rs1583686 | 5 | 85922051 | intergenic variant | T/C | snv | 0.79 | 3 | ||||
| rs1998303 | 9 | 82800066 | intergenic variant | A/G | snv | 0.37 | 3 | ||||
| rs206833 | 1.000 | 0.040 | 2 | 31485750 | intergenic variant | G/A | snv | 0.17 | 3 | ||
| rs6684897 | 1.000 | 0.120 | 1 | 238128048 | intergenic variant | C/G | snv | 0.83 | 3 | ||
| rs9937036 | 16 | 16636871 | intron variant | T/A;C;G | snv | 3 | |||||
| rs2241339 | 2 | 169013785 | intron variant | C/A;T | snv | 3 | |||||
| rs72772090 | 1.000 | 0.120 | 5 | 96700607 | intron variant | G/A;C | snv | 3 | |||
| rs11976006 | 1.000 | 0.040 | 7 | 28691895 | intron variant | G/A | snv | 6.1E-02 | 3 | ||
| rs147481775 | 1.000 | 0.120 | 22 | 31829377 | intron variant | C/A | snv | 6.6E-03 | 3 | ||
| rs13395911 | 2 | 232655544 | intron variant | A/T | snv | 0.59 | 3 | ||||
| rs149940960 | 1.000 | 0.120 | 2 | 11641492 | 3 prime UTR variant | T/C | snv | 1.0E-02 | 3 | ||
| rs34531324 | 1.000 | 0.120 | 5 | 174435441 | intron variant | A/T | snv | 0.16 | 3 | ||
| rs6550253 | 1.000 | 0.120 | 3 | 34149739 | intron variant | G/A | snv | 0.12 | 3 | ||
| rs74709575 | 1.000 | 0.120 | 13 | 38041119 | intron variant | A/C | snv | 3.1E-03 | 3 | ||
| rs4896310 | 1.000 | 0.120 | 6 | 138018697 | intergenic variant | A/G;T | snv | 3 | |||
| rs74913549 | 11 | 94180526 | intron variant | T/A;C | snv | 3 | |||||
| rs637868 | 1.000 | 0.120 | 1 | 119714487 | splice region variant | T/C | snv | 0.56 | 3 | ||
| rs12500824 | 1.000 | 0.040 | 4 | 76495474 | intron variant | A/G;T | snv | 3 |