Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2235544 | 0.742 | 0.240 | 1 | 53909897 | intron variant | C/A;T | snv | 0.53; 4.0E-06 | 14 | ||
rs7860634 | 9 | 136197833 | intron variant | G/A | snv | 0.55 | 4 | ||||
rs11726248 | 4 | 170132368 | intergenic variant | G/A | snv | 6.8E-02 | 3 | ||||
rs6499766 | 16 | 55570216 | intron variant | A/T | snv | 0.54 | 3 | ||||
rs7045138 | 9 | 97829181 | intron variant | C/G;T | snv | 3 | |||||
rs7240777 | 18 | 73500517 | intergenic variant | G/A | snv | 0.53 | 3 | ||||
rs58926603 | 17 | 6438550 | upstream gene variant | A/G | snv | 0.47 | 2 |