| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs9614162 | 1.000 | 0.080 | 22 | 30208113 | upstream gene variant | G/A | snv | 0.30 | 1 | ||
| rs2023683 | 1.000 | 0.080 | 22 | 30203607 | intron variant | G/A | snv | 0.22 | 1 | ||
| rs9614157 | 1.000 | 0.080 | 22 | 30201821 | intron variant | A/G | snv | 0.26 | 1 | ||
| rs9614158 | 1.000 | 0.080 | 22 | 30201891 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs2508049 | 1.000 | 0.080 | 6 | 29856106 | intron variant | A/G | snv | 0.11 | 1 | ||
| rs116895242 | 1.000 | 0.080 | 7 | 124306349 | intron variant | T/A | snv | 2.6E-02 | 1 | ||
| rs9343676 | 1.000 | 0.080 | 6 | 77839560 | intron variant | C/A;T | snv | 0.24 | 1 | ||
| rs200426271 | 1.000 | 0.080 | 22 | 29948468 | intron variant | -/G | ins | 1 | |||
| rs2017677 | 1.000 | 0.080 | 22 | 29987273 | non coding transcript exon variant | G/C;T | snv | 1 | |||
| rs2412963 | 1.000 | 0.080 | 22 | 29995292 | non coding transcript exon variant | G/A | snv | 0.74 | 1 | ||
| rs36590 | 1.000 | 0.080 | 22 | 29932081 | intron variant | T/A;C | snv | 1 | |||
| rs36594 | 1.000 | 0.080 | 22 | 29938393 | intron variant | C/T | snv | 0.78 | 1 | ||
| rs36604 | 1.000 | 0.080 | 22 | 29944149 | intron variant | C/A;T | snv | 0.80 | 1 | ||
| rs36606 | 1.000 | 0.080 | 22 | 29944421 | intron variant | A/T | snv | 0.80 | 1 | ||
| rs36609 | 1.000 | 0.080 | 22 | 29948468 | intron variant | T/G | snv | 0.74 | 1 | ||
| rs3788423 | 1.000 | 0.080 | 22 | 29995001 | non coding transcript exon variant | T/C | snv | 0.78 | 1 | ||
| rs3887275 | 1.000 | 0.080 | 22 | 29904123 | intron variant | C/G | snv | 0.22 | 1 | ||
| rs4239932 | 1.000 | 0.080 | 22 | 29972395 | intron variant | T/G | snv | 0.78 | 1 | ||
| rs4823063 | 1.000 | 0.080 | 22 | 29912791 | intron variant | G/C | snv | 0.21 | 1 | ||
| rs8136147 | 1.000 | 0.080 | 22 | 29908245 | intron variant | C/T | snv | 0.22 | 1 | ||
| rs9625874 | 1.000 | 0.080 | 22 | 29892636 | intron variant | A/G | snv | 0.21 | 1 | ||
| rs41172 | 1.000 | 0.080 | 22 | 30026876 | 3 prime UTR variant | T/C | snv | 0.28 | 1 | ||
| rs1245371 | 1.000 | 0.080 | 6 | 30070575 | 3 prime UTR variant | A/G | snv | 0.23 | 1 | ||
| rs142771326 | 1.000 | 0.080 | 11 | 111766340 | missense variant | C/G;T | snv | 2.0E-04 | 5.2E-04 | 1 | |
| rs973682124 | 1.000 | 0.080 | 11 | 111743419 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 |