| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13356494 | 1.000 | 0.040 | 5 | 135991866 | regulatory region variant | C/G;T | snv | 1 | |||
| rs1418688 | 1.000 | 0.040 | 6 | 71169166 | downstream gene variant | A/G;T | snv | 1 | |||
| rs17260539 | 1.000 | 0.040 | 9 | 12182545 | intergenic variant | G/A | snv | 6.6E-02 | 1 | ||
| rs1819741 | 1.000 | 0.040 | 1 | 192815708 | intron variant | T/A;C | snv | 1 | |||
| rs37790 | 1.000 | 0.040 | 5 | 53346682 | intergenic variant | C/G;T | snv | 1 | |||
| rs4145262 | 1.000 | 0.040 | 12 | 105659532 | regulatory region variant | C/A | snv | 4.8E-02 | 1 | ||
| rs4448731 | 1.000 | 0.040 | 12 | 71935326 | upstream gene variant | T/C | snv | 0.40 | 1 | ||
| rs685012 | 1.000 | 0.040 | 12 | 50052620 | upstream gene variant | C/T | snv | 0.66 | 1 | ||
| rs7301616 | 1.000 | 0.040 | 12 | 60214608 | intron variant | C/T | snv | 0.96 | 1 | ||
| rs9372078 | 1.000 | 0.040 | 6 | 150592825 | intergenic variant | T/A | snv | 0.73 | 1 | ||
| rs10875995 | 1.000 | 0.040 | 12 | 50068355 | intron variant | T/A;C | snv | 1 | |||
| rs887230 | 1.000 | 0.040 | 17 | 34577567 | non coding transcript exon variant | C/T | snv | 0.82 | 0.85 | 1 | |
| rs887231 | 1.000 | 0.040 | 17 | 34577461 | non coding transcript exon variant | G/A | snv | 0.73 | 1 | ||
| rs11763020 | 1.000 | 0.040 | 7 | 1020652 | intron variant | C/T | snv | 0.12 | 1 | ||
| rs941184 | 1.000 | 0.040 | 12 | 53720374 | intron variant | C/T | snv | 3.6E-02 | 1 | ||
| rs2039391 | 1.000 | 0.040 | 9 | 20714015 | intron variant | C/T | snv | 0.86 | 1 | ||
| rs4977831 | 1.000 | 0.040 | 9 | 20713069 | intron variant | A/G;T | snv | 1 | |||
| rs2241165 | 1.000 | 0.040 | 2 | 170821869 | non coding transcript exon variant | C/T | snv | 0.63 | 1 | ||
| rs191260602 | 1.000 | 0.040 | 4 | 157140489 | intron variant | A/G | snv | 7.7E-03 | 1 | ||
| rs2770292 | 1.000 | 0.040 | 13 | 46860971 | intron variant | C/G | snv | 0.18 | 1 | ||
| rs3742278 | 1.000 | 0.040 | 13 | 46845442 | intron variant | A/G | snv | 0.19 | 1 | ||
| rs324891 | 1.000 | 0.040 | 5 | 88616114 | intron variant | C/T | snv | 4.2E-04 | 1 | ||
| rs9302001 | 1.000 | 0.040 | 13 | 94811138 | intergenic variant | C/A;T | snv | 1 | |||
| rs10801152 | 1.000 | 0.040 | 1 | 192792174 | intron variant | A/T | snv | 0.31 | 1 | ||
| rs12061304 | 1.000 | 0.040 | 1 | 110695063 | intergenic variant | A/G | snv | 0.30 | 1 |