Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1027702 | 0.882 | 0.080 | 1 | 161743067 | intergenic variant | C/T | snv | 0.51 | 3 | ||
rs11247957 | 0.882 | 0.080 | 1 | 26429683 | 3 prime UTR variant | G/A | snv | 0.21 | 3 | ||
rs1301478248 | 0.882 | 0.080 | 1 | 15495395 | missense variant | C/T | snv | 3 | |||
rs138085133 | 0.882 | 0.080 | 1 | 26022729 | missense variant | C/G;T | snv | 8.4E-04; 4.0E-06 | 3 | ||
rs1045485 | 0.637 | 0.480 | 2 | 201284866 | missense variant | G/A;C;T | snv | 4.0E-06; 9.0E-02 | 34 | ||
rs281864719 | 0.763 | 0.240 | 2 | 29220831 | missense variant | A/C;G;T | snv | 14 | |||
rs1057519697 | 0.776 | 0.120 | 2 | 29220830 | missense variant | A/C | snv | 12 | |||
rs113994087 | 0.827 | 0.120 | 2 | 29209798 | missense variant | C/A;T | snv | 12 | |||
rs863225281 | 0.776 | 0.200 | 2 | 29220829 | missense variant | G/C;T | snv | 12 | |||
rs121908513 | 0.807 | 0.280 | 2 | 32116145 | missense variant | T/A | snv | 6 | |||
rs1048108 | 0.827 | 0.120 | 2 | 214809500 | missense variant | G/A | snv | 0.38 | 0.33 | 5 | |
rs57961569 | 0.827 | 0.200 | 2 | 15939643 | intron variant | G/A;C | snv | 5 | |||
rs6435862 | 0.827 | 0.160 | 2 | 214807822 | intron variant | G/A;C;T | snv | 5 | |||
rs863225285 | 0.851 | 0.080 | 2 | 29209789 | missense variant | T/G | snv | 5 | |||
rs3768716 | 0.851 | 0.080 | 2 | 214771070 | intron variant | T/C | snv | 0.16 | 4 | ||
rs535080528 | 0.851 | 0.120 | 2 | 69431903 | splice region variant | T/A;C | snv | 4.0E-06 | 4 | ||
rs13034994 | 0.882 | 0.080 | 2 | 15938513 | non coding transcript exon variant | A/C;G | snv | 3 | |||
rs1442511697 | 0.882 | 0.080 | 2 | 96115494 | missense variant | T/C | snv | 7.0E-06 | 3 | ||
rs17487792 | 0.882 | 0.080 | 2 | 214778776 | intron variant | C/T | snv | 0.16 | 3 | ||
rs17489363 | 0.882 | 0.080 | 2 | 214809617 | 5 prime UTR variant | A/G | snv | 0.73 | 0.74 | 3 | |
rs2302616 | 0.882 | 0.080 | 2 | 10448065 | intron variant | C/A | snv | 0.26 | 3 | ||
rs3738888 | 0.882 | 0.080 | 2 | 214730440 | missense variant | G/A;T | snv | 8.4E-03 | 3 | ||
rs3768707 | 0.882 | 0.080 | 2 | 214780411 | intron variant | A/G | snv | 0.74 | 3 | ||
rs60226897 | 0.882 | 0.080 | 2 | 15947252 | downstream gene variant | G/A | snv | 4.3E-02 | 3 | ||
rs9653226 | 0.882 | 0.080 | 2 | 15939632 | intron variant | C/T | snv | 0.54 | 3 |