| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2030519 | 0.827 | 0.200 | 3 | 188402113 | intron variant | G/A | snv | 0.61 | 7 | ||
| rs4459895 | 0.827 | 0.160 | 3 | 188236626 | intron variant | A/C | snv | 0.88 | 5 | ||
| rs9860547 | 0.925 | 0.080 | 3 | 188411191 | intron variant | G/A | snv | 0.34 | 3 | ||
| rs11719821 | 0.882 | 0.040 | 3 | 188370530 | intron variant | T/C | snv | 0.36 | 3 | ||
| rs191177147 | 0.882 | 0.040 | 3 | 188374758 | intron variant | G/T | snv | 3 | |||
| rs13093110 | 0.882 | 0.120 | 3 | 188407332 | intron variant | C/T | snv | 0.42 | 3 | ||
| rs9815073 | 0.925 | 0.120 | 3 | 188397894 | intron variant | C/A;G | snv | 3 | |||
| rs73196739 | 0.925 | 0.120 | 3 | 188684683 | intron variant | C/T | snv | 0.13 | 2 | ||
| rs55661102 | 0.925 | 0.080 | 3 | 188683350 | intron variant | A/G | snv | 0.13 | 2 | ||
| rs17670280 | 1.000 | 0.080 | 3 | 188682451 | intron variant | G/A;C | snv | 2 | |||
| rs13099273 | 1.000 | 0.080 | 3 | 188415730 | intron variant | A/G;T | snv | 2 | |||
| rs1464510 | 0.807 | 0.280 | 3 | 188394766 | intron variant | C/A;T | snv | 2 | |||
| rs56116661 | 1.000 | 0.040 | 3 | 188683372 | intron variant | C/T | snv | 0.25 | 2 | ||
| rs60946162 | 1.000 | 0.040 | 3 | 188415548 | intron variant | C/T | snv | 0.35 | 2 | ||
| rs149437411 | 3 | 188609231 | missense variant | C/G;T | snv | 4.0E-06; 1.9E-03 | 2 | ||||
| rs12634152 | 0.925 | 0.120 | 3 | 188403231 | intron variant | C/T | snv | 0.43 | 2 | ||
| rs542618547 | 3 | 188728876 | intron variant | AAA/-;A;AA;AAAA;AAAAA | delins | 0.23 | 2 | ||||
| rs9864529 | 1.000 | 0.040 | 3 | 188387268 | intron variant | G/A | snv | 0.52 | 1 | ||
| rs73194495 | 1.000 | 0.080 | 3 | 188610688 | intron variant | A/T | snv | 0.15 | 1 | ||
| rs9852988 | 1.000 | 0.080 | 3 | 188327228 | intron variant | A/G | snv | 0.11 | 1 | ||
| rs2889896 | 1.000 | 0.080 | 3 | 188384928 | intron variant | C/T | snv | 0.43 | 1 | ||
| rs3856920 | 3 | 188823038 | intron variant | A/G | snv | 0.25 | 1 | ||||
| rs4686952 | 3 | 188331054 | intron variant | G/A | snv | 0.43 | 1 | ||||
| rs4686991 | 3 | 188647490 | intron variant | A/G;T | snv | 1 | |||||
| rs6444307 | 3 | 188589730 | intron variant | A/G | snv | 0.33 | 1 |