Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 47 | ||
| rs334 | 0.724 | 0.240 | 11 | 5227002 | missense variant | T/A;C;G | snv | 3.5E-03 | 35 | ||
| rs13331259 | 16 | 249924 | intron variant | A/G | snv | 3.0E-02 | 14 | ||||
| rs7775698 | 1.000 | 0.080 | 6 | 135097497 | intron variant | C/T | snv | 6.9E-02 | 14 | ||
| rs112505971 | 10 | 27068541 | intron variant | A/C;G | snv | 13 | |||||
| rs2853961 | 6 | 31264212 | downstream gene variant | G/A | snv | 0.38 | 13 | ||||
| rs3123543 | 1 | 212617344 | intron variant | T/A;C | snv | 13 | |||||
| rs3840870 | 17 | 50184820 | 3 prime UTR variant | -/CTTG | delins | 13 | |||||
| rs4837892 | 9 | 121826025 | intron variant | G/T | snv | 0.36 | 13 | ||||
| rs603424 | 1.000 | 0.080 | 10 | 100315722 | intron variant | G/A | snv | 0.34 | 13 | ||
| rs7296503 | 12 | 41306962 | intron variant | C/T | snv | 0.57 | 13 | ||||
| rs76792961 | 16 | 243594 | intron variant | C/T | snv | 7.3E-03 | 13 | ||||
| rs9917425 | 20 | 16755400 | intron variant | G/T | snv | 0.16 | 13 | ||||
| rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 | |||||
| rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
| rs35979828 | 12 | 54292096 | intron variant | C/T | snv | 5.0E-02 | 9 | ||||
| rs34651 | 1.000 | 0.040 | 5 | 72848178 | non coding transcript exon variant | C/T | snv | 0.94 | 5 | ||
| rs7394579 | 1.000 | 0.080 | 11 | 61813978 | intron variant | A/G | snv | 0.22 | 5 | ||
| rs11734132 | 4 | 6889792 | intergenic variant | G/C | snv | 0.17 | 3 | ||||
| rs2157770 | 9 | 134056342 | intron variant | A/G | snv | 0.33 | 3 | ||||
| rs3842397 | 18 | 46265918 | 3 prime UTR variant | TT/- | del | 0.43 | 3 |