Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397516436 | 0.641 | 0.440 | 17 | 7674894 | stop gained | G/A;C | snv | 34 | |||
rs786201059 | 0.701 | 0.360 | 17 | 7673764 | stop gained | C/A;G;T | snv | 20 | |||
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 71 | ||
rs104894226 | 0.658 | 0.560 | 11 | 534285 | missense variant | C/A;G;T | snv | 29 | |||
rs104894228 | 0.605 | 0.560 | 11 | 534286 | missense variant | C/A;G;T | snv | 48 | |||
rs104894229 | 0.564 | 0.600 | 11 | 534289 | missense variant | C/A;G;T | snv | 73 | |||
rs104894230 | 0.564 | 0.600 | 11 | 534288 | missense variant | C/A;G;T | snv | 73 | |||
rs1057519045 | 0.851 | 0.160 | 10 | 121498522 | missense variant | T/G | snv | 6 | |||
rs1057519747 | 0.716 | 0.280 | 17 | 7675094 | missense variant | A/C;G;T | snv | 23 | |||
rs1057519787 | 1.000 | 0.040 | 17 | 39711952 | missense variant | G/A;C | snv | 2 | |||
rs1057519816 | 0.763 | 0.200 | 17 | 39711955 | missense variant | C/A;T | snv | 14 | |||
rs1057519854 | 0.882 | 0.080 | 10 | 121488063 | missense variant | A/T | snv | 7 | |||
rs1057519895 | 0.724 | 0.240 | 4 | 152328232 | missense variant | C/A;G;T | snv | 17 | |||
rs1057519901 | 0.925 | 0.080 | 10 | 121498525 | missense variant | T/G | snv | 5 | |||
rs1057519925 | 0.683 | 0.560 | 3 | 179210291 | missense variant | G/A;C | snv | 25 | |||
rs1057519926 | 0.776 | 0.200 | 3 | 179210293 | missense variant | A/T | snv | 10 | |||
rs1057519927 | 0.716 | 0.240 | 3 | 179218295 | missense variant | A/C;G;T | snv | 19 | |||
rs1057519928 | 0.807 | 0.200 | 3 | 179221147 | missense variant | A/C | snv | 8 | |||
rs1057519929 | 0.776 | 0.320 | 3 | 179199066 | missense variant | G/A | snv | 10 | |||
rs1057519932 | 0.683 | 0.320 | 3 | 179234298 | missense variant | T/G | snv | 22 | |||
rs1057519933 | 0.790 | 0.240 | 3 | 179199156 | missense variant | A/G | snv | 11 | |||
rs1057519934 | 0.790 | 0.240 | 3 | 179199158 | missense variant | G/C | snv | 11 | |||
rs1057519935 | 0.790 | 0.240 | 3 | 179199157 | missense variant | A/G | snv | 11 | |||
rs1057519938 | 0.776 | 0.160 | 3 | 179203764 | missense variant | A/C;T | snv | 10 |