| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2395029 | 0.790 | 0.320 | 6 | 31464003 | non coding transcript exon variant | T/G | snv | 2.7E-02 | 2.4E-02 | 7 | |
| rs1495741 | 0.827 | 0.240 | 8 | 18415371 | regulatory region variant | G/A | snv | 0.71 | 3 | ||
| rs3129900 | 0.882 | 0.200 | 6 | 32338202 | intron variant | G/T | snv | 0.83 | 3 | ||
| rs9274407 | 0.925 | 0.120 | 6 | 32665055 | missense variant | A/C;T | snv | 0.77 | 2 | ||
| rs10812428 | 1.000 | 0.080 | 9 | 26614849 | intergenic variant | C/T | snv | 0.40 | 1 | ||
| rs2523822 | 1.000 | 0.080 | 6 | 29860883 | intron variant | A/G | snv | 0.26 | 1 | ||
| rs6582630 | 1.000 | 0.080 | 12 | 38349706 | intergenic variant | G/A | snv | 0.62 | 1 | ||
| rs1497546 | 1.000 | 0.080 | 3 | 98315682 | intron variant | G/A | snv | 9.0E-02 | 1 | ||
| rs17036170 | 1.000 | 0.080 | 3 | 12288912 | 5 prime UTR variant | G/A | snv | 1.1E-02 | 1 | ||
| rs10937275 | 1.000 | 0.080 | 3 | 186933001 | intron variant | A/G | snv | 0.88 | 1 |