| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11221332 | 0.763 | 0.280 | 11 | 128511079 | intron variant | C/A;T | snv | 8 | |||
| rs11221322 | 0.827 | 0.120 | 11 | 128476898 | intron variant | T/C | snv | 0.13 | 5 | ||
| rs8705 | 11 | 128459018 | 3 prime UTR variant | G/A;T | snv | 5 | |||||
| rs7924522 | 1.000 | 0.040 | 11 | 128510847 | intron variant | C/A | snv | 0.70 | 2 | ||
| rs3802826 | 0.925 | 0.040 | 11 | 128536543 | non coding transcript exon variant | A/G;T | snv | 2 | |||
| rs34834119 | 11 | 128463122 | intron variant | AT/- | del | 0.26 | 2 | ||||
| rs4128561 | 1.000 | 0.080 | 11 | 128545234 | intron variant | T/C | snv | 0.58 | 1 | ||
| rs11819995 | 1.000 | 0.080 | 11 | 128519496 | intron variant | C/T | snv | 0.23 | 1 | ||
| rs1128334 | 0.851 | 0.160 | 11 | 128459064 | 3 prime UTR variant | C/T | snv | 0.11 | 1 | ||
| rs3809006 | 1.000 | 0.080 | 11 | 128540941 | intron variant | C/G;T | snv | 1 | |||
| rs4937333 | 0.882 | 0.120 | 11 | 128460625 | 3 prime UTR variant | T/C | snv | 0.45 | 1 | ||
| rs6590334 | 1.000 | 0.040 | 11 | 128533313 | intron variant | T/C | snv | 0.60 | 1 | ||
| rs7108992 | 11 | 128511972 | intron variant | A/C | snv | 0.71 | 1 | ||||
| rs4937334 | 11 | 128465683 | intron variant | G/A | snv | 0.22 | 1 | ||||
| rs116502295 | 1.000 | 11 | 128462620 | intron variant | T/C | snv | 6.1E-03 | 7.1E-03 | 1 | ||
| rs67232546 | 1.000 | 0.080 | 11 | 128529043 | non coding transcript exon variant | C/T | snv | 0.17 | 1 | ||
| rs11221357 | 11 | 128574116 | intron variant | C/T | snv | 0.35 | 1 | ||||
| rs61907765 | 1.000 | 0.080 | 11 | 128522042 | 5 prime UTR variant | C/G;T | snv | 0.17 | 0.15 | 1 |