Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1126809 | 0.683 | 0.320 | 11 | 89284793 | missense variant | G/A | snv | 0.18 | 0.18 | 29 | |
rs28940877 | 0.807 | 0.200 | 11 | 89178218 | missense variant | T/C | snv | 4.0E-06 | 2.1E-05 | 9 | |
rs104894313 | 0.807 | 0.160 | 11 | 89284805 | missense variant | C/T | snv | 3.8E-03; 4.0E-06 | 3.7E-03 | 7 | |
rs376823382 | 0.827 | 0.200 | 11 | 89284940 | missense variant | A/G | snv | 1.9E-04 | 2.2E-04 | 8 | |
rs121908011 | 0.827 | 0.160 | 11 | 89227933 | missense variant | G/A | snv | 9.2E-05 | 3.5E-05 | 6 | |
rs1376096651 | 0.882 | 0.280 | 3 | 69964977 | missense variant | A/G;T | snv | 3 | |||
rs1057518787 | 0.925 | 0.200 | X | 9765782 | frameshift variant | CAGCAGAAGGTCCCTAGGCGCGGGG/- | delins | 3 | |||
rs1057518763 | 1.000 | 0.160 | 11 | 89178026 | frameshift variant | -/T | delins | 7.0E-06 | 1 | ||
rs1057518841 | 1.000 | 0.160 | 9 | 12695799 | missense variant | C/T | snv | 1 | |||
rs771055145 | 1.000 | 0.160 | 9 | 12704577 | missense variant | A/G | snv | 2.0E-05 | 7.0E-06 | 1 |