| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 7 | ||
| rs61816761 | 0.658 | 0.640 | 1 | 152313385 | stop gained | G/A;T | snv | 9.4E-03; 8.0E-06 | 5 | ||
| rs7512552 | 1.000 | 0.120 | 1 | 150293284 | upstream gene variant | T/C | snv | 0.63 | 4 | ||
| rs12081541 | 0.925 | 0.160 | 1 | 152468890 | intergenic variant | T/C | snv | 8.9E-02 | 2 | ||
| rs12130219 | 0.925 | 0.120 | 1 | 152189630 | non coding transcript exon variant | A/G | snv | 0.23 | 2 | ||
| rs4363385 | 0.925 | 0.120 | 1 | 153016845 | upstream gene variant | T/C | snv | 0.62 | 2 | ||
| rs6684514 | 0.925 | 0.120 | 1 | 156285665 | missense variant | G/A | snv | 0.27 | 0.24 | 2 | |
| rs10888499 | 1.000 | 0.120 | 1 | 152560266 | intergenic variant | C/A;T | snv | 1 | |||
| rs11205006 | 1.000 | 0.120 | 1 | 152467700 | intergenic variant | A/T | snv | 0.72 | 1 | ||
| rs12144049 | 1.000 | 0.120 | 1 | 152468434 | intergenic variant | C/G;T | snv | 1 | |||
| rs3126085 | 0.851 | 0.280 | 1 | 152328341 | intron variant | G/A | snv | 0.29 | 1 | ||
| rs471144 | 1.000 | 0.120 | 1 | 152481779 | intergenic variant | T/G | snv | 8.0E-02 | 1 | ||
| rs55879323 | 1.000 | 0.120 | 1 | 152196264 | intron variant | C/T | snv | 0.42 | 1 | ||
| rs61813875 | 1.000 | 0.120 | 1 | 152564174 | downstream gene variant | C/G | snv | 1.6E-02 | 1 | ||
| rs6661961 | 1.000 | 0.120 | 1 | 152469813 | intergenic variant | T/A;C | snv | 1 | |||
| rs6686734 | 1.000 | 0.120 | 1 | 12008884 | intron variant | T/C | snv | 0.71 | 1 | ||
| rs77199844 | 1.000 | 0.120 | 1 | 152784619 | upstream gene variant | AT/- | del | 0.12 | 1 | ||
| rs13015714 | 0.882 | 0.200 | 2 | 102355405 | intron variant | G/T | snv | 0.77 | 2 | ||
| rs3917265 | 1.000 | 0.120 | 2 | 102162001 | intron variant | T/C | snv | 0.50 | 2 | ||
| rs62176107 | 0.925 | 0.120 | 2 | 178436244 | missense variant | G/A;T | snv | 2 | |||
| rs6548123 | 0.925 | 0.120 | 2 | 2221629 | intron variant | C/T | snv | 0.76 | 2 | ||
| rs67766926 | 0.925 | 0.120 | 2 | 60936446 | downstream gene variant | C/G | snv | 0.17 | 2 | ||
| rs10199605 | 1.000 | 0.120 | 2 | 8354967 | intron variant | G/A | snv | 0.26 | 1 | ||
| rs112111458 | 0.925 | 0.120 | 2 | 70872975 | intergenic variant | A/G | snv | 0.16 | 1 | ||
| rs2271404 | 1.000 | 0.120 | 2 | 111246290 | non coding transcript exon variant | T/C | snv | 0.12 | 1 |