| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2618476 | 0.925 | 0.160 | 8 | 11495032 | intron variant | T/C | snv | 0.26 | 2 | ||
| rs13277113 | 0.695 | 0.520 | 8 | 11491677 | intron variant | G/A | snv | 0.25 | 2 | ||
| rs2248932 | 0.882 | 0.160 | 8 | 11534141 | intron variant | A/G | snv | 0.60 | 1 | ||
| rs4840568 | 0.882 | 0.160 | 8 | 11493510 | intron variant | G/A | snv | 0.32 | 1 | ||
| rs6993775 | 1.000 | 0.120 | 8 | 11512480 | intron variant | G/T | snv | 0.77 | 1 | ||
| rs2251056 | 1.000 | 0.120 | 8 | 11492067 | intron variant | C/A | snv | 0.83 | 1 | ||
| rs2736354 | 1.000 | 0.120 | 8 | 11511222 | intron variant | T/C | snv | 0.83 | 1 | ||
| rs2618457 | 1.000 | 0.120 | 8 | 11511668 | intron variant | A/G | snv | 0.85 | 1 | ||
| rs1382568 | 0.925 | 0.160 | 8 | 11493711 | intron variant | A/C;G | snv | 1 | |||
| rs2618469 | 1.000 | 0.120 | 8 | 11501871 | intron variant | G/A | snv | 0.84 | 1 | ||
| rs2736353 | 1.000 | 0.120 | 8 | 11509529 | non coding transcript exon variant | C/T | snv | 0.84 | 1 | ||
| rs2618458 | 1.000 | 0.120 | 8 | 11511559 | intron variant | A/C;G;T | snv | 1 | |||
| rs2618467 | 1.000 | 0.120 | 8 | 11504734 | intron variant | T/C | snv | 0.86 | 1 | ||
| rs9694294 | 1.000 | 0.120 | 8 | 11493212 | intron variant | C/G | snv | 0.82 | 1 | ||
| rs922483 | 0.882 | 0.200 | 8 | 11494403 | 5 prime UTR variant | C/T | snv | 0.31 | 1 | ||
| rs10100215 | 1.000 | 0.120 | 8 | 11504763 | intron variant | G/T | snv | 0.26 | 1 | ||
| rs1478887 | 1.000 | 0.120 | 8 | 11498471 | intron variant | C/T | snv | 0.64 | 1 | ||
| rs9693589 | 1.000 | 0.120 | 8 | 11491452 | intron variant | G/A;C | snv | 1 | |||
| rs4840565 | 1.000 | 0.120 | 8 | 11488036 | intron variant | G/C | snv | 0.33 | 1 | ||
| rs2250788 | 1.000 | 0.120 | 8 | 11494547 | 5 prime UTR variant | A/G;T | snv | 1 | |||
| rs2618455 | 1.000 | 0.120 | 8 | 11513369 | intron variant | A/G;T | snv | 1 | |||
| rs2736350 | 1.000 | 0.120 | 8 | 11504043 | intron variant | T/G | snv | 0.41 | 1 | ||
| rs569648905 | 1.000 | 0.120 | 8 | 11511223 | intron variant | C/- | del | 1 | |||
| rs2736344 | 1.000 | 0.120 | 8 | 11493169 | intron variant | T/C;G | snv | 1 | |||
| rs2618471 | 1.000 | 0.120 | 8 | 11501511 | intron variant | C/G | snv | 0.37 | 1 |