Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121908120 | 0.701 | 0.280 | 2 | 218890289 | missense variant | T/A | snv | 1.4E-02 | 1.4E-02 | 19 | |
rs147680216 | 0.742 | 0.160 | 2 | 218890244 | missense variant | G/A | snv | 2.1E-03 | 6.9E-04 | 11 | |
rs121908119 | 0.763 | 0.200 | 2 | 218882368 | stop gained | C/A | snv | 6.2E-04 | 8.5E-04 | 10 | |
rs374910216 | 0.882 | 0.080 | 2 | 218882358 | missense variant | G/A | snv | 2.4E-05 | 3 | ||
rs1060499588 | 0.882 | 0.200 | 2 | 218890223 | stop gained | C/T | snv | 3 | |||
rs116998555 | 0.882 | 0.080 | 2 | 218890118 | missense variant | C/A;T | snv | 4.0E-06; 1.9E-03 | 3 | ||
rs372993798 | 0.882 | 0.200 | 2 | 218889998 | missense variant | G/A;T | snv | 3.6E-05; 4.0E-06 | 3 | ||
rs750190755 | 0.882 | 0.080 | 2 | 218893087 | missense variant | C/T | snv | 4.1E-05 | 7.0E-06 | 3 | |
rs762739726 | 0.882 | 0.200 | 2 | 218889989 | stop gained | C/T | snv | 1.6E-05 | 3 | ||
rs121908121 | 0.925 | 0.120 | 2 | 218889990 | missense variant | G/A | snv | 7.6E-05 | 9.1E-05 | 2 | |
rs886039453 | 0.925 | 0.120 | 2 | 218890349 | stop gained | C/T | snv | 8.4E-06 | 2.1E-05 | 2 | |
rs141074983 | 1.000 | 0.080 | 2 | 218882384 | missense variant | C/A;T | snv | 4.0E-06; 8.6E-04 | 1 | ||
rs146460077 | 1.000 | 0.080 | 2 | 218882255 | missense variant | C/T | snv | 1.8E-03 | 9.9E-04 | 1 | |
rs318240759 | 1.000 | 0.080 | 2 | 218882330 | missense variant | G/A | snv | 1.2E-05 | 1.4E-05 | 1 | |
rs1234227647 | 1.000 | 0.080 | 2 | 218892848 | missense variant | G/T | snv | 1.4E-05 | 1 | ||
rs1347556761 | 1.000 | 0.080 | 2 | 218893152 | missense variant | C/T | snv | 4.7E-06 | 1.4E-05 | 1 | |
rs146902156 | 1.000 | 0.080 | 2 | 218890256 | missense variant | G/A | snv | 3.9E-04 | 2.9E-04 | 1 | |
rs149245953 | 1.000 | 0.080 | 2 | 218890274 | missense variant | C/A;T | snv | 2.0E-05; 4.1E-06; 6.1E-05 | 1 | ||
rs202024965 | 1.000 | 0.080 | 2 | 218890034 | missense variant | C/A;T | snv | 2.5E-04 | 1.0E-04 | 1 | |
rs368280129 | 1.000 | 0.080 | 2 | 218890094 | missense variant | C/G;T | snv | 4.0E-06; 1.1E-04 | 1 | ||
rs543063101 | 1.000 | 0.080 | 2 | 218890040 | missense variant | G/A;C;T | snv | 5.6E-05; 2.8E-05 | 1 | ||
rs745513263 | 1.000 | 0.080 | 2 | 218892935 | missense variant | C/G;T | snv | 5.2E-04 | 1 | ||
rs778752861 | 1.000 | 0.080 | 2 | 218892813 | missense variant | G/A | snv | 4.8E-06 | 1 | ||
rs1245189224 | 1.000 | 0.080 | 2 | 218882423 | missense variant | G/A | snv | 4.0E-06 | 1 |