Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs907715 | 0.752 | 0.520 | 4 | 122613898 | intron variant | C/T | snv | 0.35 | 11 | ||
rs2248462 | 0.807 | 0.240 | 6 | 31479019 | downstream gene variant | G/A | snv | 0.19 | 10 | ||
rs11594656 | 0.776 | 0.240 | 10 | 6080046 | intergenic variant | T/A | snv | 0.18 | 9 | ||
rs2516509 | 0.882 | 0.160 | 6 | 31482217 | intron variant | T/C | snv | 0.19 | 7 | ||
rs9277554 | 0.790 | 0.520 | 6 | 33087761 | 3 prime UTR variant | C/T | snv | 0.38 | 7 | ||
rs3129763 | 0.827 | 0.280 | 6 | 32623148 | TF binding site variant | G/A | snv | 0.23 | 6 | ||
rs9275312 | 0.807 | 0.280 | 6 | 32697951 | intergenic variant | A/G | snv | 0.16 | 6 | ||
rs12722495 | 0.851 | 0.200 | 10 | 6055320 | intron variant | T/C | snv | 7.0E-02 | 5 | ||
rs3129871 | 0.827 | 0.320 | 6 | 32438565 | upstream gene variant | A/C | snv | 0.59 | 5 | ||
rs9296015 | 0.851 | 0.280 | 6 | 32251212 | upstream gene variant | G/A | snv | 0.22 | 4 | ||
rs2516398 | 0.882 | 0.200 | 6 | 31513749 | upstream gene variant | G/T | snv | 0.70 | 3 | ||
rs2856705 | 0.882 | 0.200 | 6 | 32703179 | downstream gene variant | C/T | snv | 0.11 | 3 | ||
rs3117230 | 0.882 | 0.200 | 6 | 33107858 | upstream gene variant | A/G | snv | 0.28 | 3 | ||
rs479536 | 0.882 | 0.200 | 6 | 32225901 | upstream gene variant | G/A | snv | 5.0E-02 | 3 | ||
rs2844494 | 0.925 | 0.160 | 6 | 31515638 | upstream gene variant | C/A | snv | 0.70 | 2 |