| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs711752 | 1.000 | 0.040 | 16 | 56962299 | splice region variant | G/A;C | snv | 10 | |||
| rs9987289 | 1.000 | 0.040 | 8 | 9325848 | non coding transcript exon variant | A/G | snv | 0.87 | 10 | ||
| rs17863787 | 0.925 | 0.040 | 2 | 233702448 | intron variant | T/G | snv | 0.30 | 9 | ||
| rs929596 | 0.925 | 0.040 | 2 | 233765830 | intron variant | A/G | snv | 0.32 | 9 | ||
| rs10096633 | 1.000 | 0.040 | 8 | 19973410 | regulatory region variant | C/T | snv | 0.22 | 8 | ||
| rs7350481 | 0.882 | 0.040 | 11 | 116715567 | regulatory region variant | T/C | snv | 0.93 | 8 | ||
| rs17410962 | 1.000 | 0.040 | 8 | 19990569 | intergenic variant | G/A | snv | 0.15 | 7 | ||
| rs12286037 | 1.000 | 0.040 | 11 | 116781491 | intron variant | C/T | snv | 0.11 | 6 | ||
| rs12686004 | 1.000 | 0.040 | 9 | 104891145 | intron variant | G/A | snv | 9.1E-02 | 6 | ||
| rs9939224 | 1.000 | 0.040 | 16 | 56968820 | intron variant | T/G | snv | 0.75 | 6 | ||
| rs11820589 | 1.000 | 0.040 | 11 | 116763146 | missense variant | G/A | snv | 7.8E-02 | 0.10 | 5 | |
| rs11986942 | 1.000 | 0.040 | 8 | 20009934 | intergenic variant | C/G;T | snv | 5 | |||
| rs17489282 | 1.000 | 0.040 | 8 | 19995007 | regulatory region variant | C/T | snv | 0.25 | 5 | ||
| rs1919484 | 1.000 | 0.040 | 8 | 20012165 | intergenic variant | G/A | snv | 0.23 | 5 | ||
| rs2160669 | 1.000 | 0.040 | 11 | 116776891 | 3 prime UTR variant | C/T | snv | 0.92 | 5 | ||
| rs481843 | 1.000 | 0.040 | 11 | 116655150 | non coding transcript exon variant | C/T | snv | 8.8E-02 | 5 | ||
| rs6494005 | 1.000 | 0.040 | 15 | 58432325 | non coding transcript exon variant | A/G | snv | 0.38 | 5 | ||
| rs11216126 | 1.000 | 0.040 | 11 | 116746524 | downstream gene variant | A/C | snv | 0.11 | 4 | ||
| rs16940212 | 1.000 | 0.040 | 15 | 58401821 | intron variant | G/A;T | snv | 4 | |||
| rs263 | 1.000 | 0.040 | 8 | 19955301 | intron variant | C/T | snv | 0.23 | 4 | ||
| rs271 | 1.000 | 0.040 | 8 | 19956191 | intron variant | G/A;T | snv | 4 | |||
| rs2741027 | 1.000 | 0.040 | 2 | 233609365 | downstream gene variant | G/A | snv | 0.22 | 4 | ||
| rs486394 | 1.000 | 0.040 | 11 | 116655605 | intron variant | A/C;T | snv | 4 | |||
| rs6589567 | 1.000 | 0.040 | 11 | 116799960 | intergenic variant | A/C;G;T | snv | 4 | |||
| rs7013777 | 1.000 | 0.040 | 8 | 20020845 | intergenic variant | T/C;G | snv | 4 |