Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 3 | |
rs887829 | 0.763 | 0.280 | 2 | 233759924 | intron variant | C/T | snv | 0.36 | 8 | ||
rs10189857 | 1.000 | 0.080 | 2 | 60486100 | intron variant | A/G | snv | 0.42 | 5 | ||
rs766432 | 0.925 | 0.080 | 2 | 60492835 | intron variant | C/A | snv | 0.80 | 5 | ||
rs6729815 | 1.000 | 0.080 | 2 | 60496537 | intron variant | T/C | snv | 0.49 | 4 | ||
rs7599488 | 0.925 | 0.120 | 2 | 60491212 | intron variant | C/T | snv | 0.42 | 4 | ||
rs7606173 | 1.000 | 0.080 | 2 | 60498316 | intron variant | G/C;T | snv | 0.39 | 4 | ||
rs4671393 | 0.790 | 0.400 | 2 | 60493816 | intron variant | A/C;G | snv | 3 | |||
rs7565301 | 1.000 | 0.080 | 2 | 60496131 | intron variant | G/A | snv | 0.25 | 3 | ||
rs10172646 | 1.000 | 0.080 | 2 | 60493622 | intron variant | G/A | snv | 0.64 | 2 | ||
rs10195871 | 1.000 | 0.080 | 2 | 60493454 | intron variant | A/G;T | snv | 2 | |||
rs11886868 | 0.752 | 0.280 | 2 | 60493111 | intron variant | C/T | snv | 0.65 | 2 | ||
rs1427407 | 0.827 | 0.120 | 2 | 60490908 | intron variant | T/C;G | snv | 2 | |||
rs1669539 | 1.000 | 0.080 | 2 | 105998818 | intergenic variant | T/C | snv | 7.1E-02 | 2 | ||
rs1896294 | 1.000 | 0.080 | 2 | 60491939 | intron variant | C/G;T | snv | 2 | |||
rs1896295 | 1.000 | 0.080 | 2 | 60496951 | intron variant | T/C | snv | 0.81 | 2 | ||
rs1896296 | 1.000 | 0.080 | 2 | 60496952 | intron variant | G/T | snv | 0.80 | 2 | ||
rs6545816 | 1.000 | 0.080 | 2 | 60487726 | intron variant | A/C;G | snv | 0.50 | 2 | ||
rs6545817 | 1.000 | 0.080 | 2 | 60488044 | intron variant | C/T | snv | 0.49 | 2 | ||
rs6706648 | 1.000 | 0.080 | 2 | 60494905 | intron variant | C/G;T | snv | 2 | |||
rs6738440 | 1.000 | 0.080 | 2 | 60495106 | intron variant | A/G | snv | 0.26 | 2 | ||
rs7557939 | 1.000 | 0.080 | 2 | 60494212 | intron variant | G/A | snv | 0.64 | 2 | ||
rs7584113 | 1.000 | 0.080 | 2 | 60494176 | intron variant | A/G | snv | 0.64 | 2 | ||
rs16944 | 0.531 | 0.920 | 2 | 112837290 | upstream gene variant | A/G | snv | 0.57 | 1 | ||
rs9714060 | 1.000 | 0.080 | 3 | 195760605 | intron variant | A/C;G | snv | 1 |