Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11554290 | 0.583 | 0.600 | 1 | 114713908 | missense variant | T/A;C;G | snv | 4 | |||
rs267607040 | 0.851 | 0.320 | 18 | 44951948 | missense variant | G/A | snv | 4 | |||
rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 3 | ||
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 3 | ||
rs104894228 | 0.605 | 0.560 | 11 | 534286 | missense variant | C/A;G;T | snv | 2 | |||
rs104894230 | 0.564 | 0.600 | 11 | 534288 | missense variant | C/A;G;T | snv | 2 | |||
rs104894366 | 0.776 | 0.400 | 12 | 25245284 | missense variant | G/A;C | snv | 2 | |||
rs112445441 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 2 | |||
rs121434595 | 0.708 | 0.320 | 1 | 114716124 | missense variant | C/A;G;T | snv | 2 | |||
rs121434596 | 0.677 | 0.440 | 1 | 114716123 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06 | 2 | ||
rs121912666 | 0.645 | 0.360 | 17 | 7674872 | missense variant | T/C;G | snv | 8.0E-06 | 2 | ||
rs121913237 | 0.611 | 0.560 | 1 | 114716126 | missense variant | C/A;G;T | snv | 8.0E-06 | 2 | ||
rs121913487 | 0.925 | 0.120 | 13 | 28018503 | missense variant | A/C;T | snv | 2 | |||
rs121913499 | 0.605 | 0.520 | 2 | 208248389 | missense variant | G/A;C;T | snv | 2 | |||
rs121913506 | 0.677 | 0.320 | 4 | 54733154 | missense variant | G/A;C;T | snv | 2 | |||
rs121913507 | 0.614 | 0.400 | 4 | 54733155 | missense variant | A/T | snv | 2 | |||
rs121918453 | 0.732 | 0.280 | 12 | 112450394 | missense variant | G/A;C;T | snv | 2 | |||
rs121918454 | 0.742 | 0.280 | 12 | 112450395 | missense variant | C/A;G;T | snv | 2 | |||
rs387906631 | 0.882 | 0.080 | 3 | 128481901 | missense variant | G/A | snv | 2 | |||
rs397507510 | 0.776 | 0.280 | 12 | 112450361 | missense variant | G/A;C;T | snv | 2 | |||
rs569067880 | 0.925 | 0.080 | 4 | 105234864 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 2 | ||
rs104894226 | 0.658 | 0.560 | 11 | 534285 | missense variant | C/A;G;T | snv | 1 | |||
rs104894229 | 0.564 | 0.600 | 11 | 534289 | missense variant | C/A;G;T | snv | 1 | |||
rs104894231 | 0.776 | 0.360 | 11 | 533467 | missense variant | C/G;T | snv | 1 | |||
rs1057519906 | 0.882 | 0.120 | 15 | 90088607 | missense variant | T/A;C | snv | 1 |