| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs33915217 | 0.752 | 0.080 | 11 | 5226925 | splice region variant | C/A;G;T | snv | 4.0E-06; 5.9E-04; 4.0E-06 | 11 | ||
| rs35004220 | 0.752 | 0.080 | 11 | 5226820 | non coding transcript exon variant | C/T | snv | 1.6E-04 | 9.1E-05 | 11 | |
| rs35256489 | 0.827 | 0.080 | 11 | 5225710 | missense variant | A/G | snv | 4.0E-06 | 2.1E-05 | 5 | |
| rs34451549 | 0.851 | 0.080 | 11 | 5225923 | intron variant | G/A | snv | 4.9E-05 | 4 | ||
| rs33960103 | 0.882 | 0.080 | 11 | 5226930 | missense variant | C/G;T | snv | 1.0E-04; 8.0E-06 | 3 |