Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121434498 | 0.807 | 0.280 | 19 | 4117553 | missense variant | A/C;G;T | snv | 6 | |||
rs1057519910 | 0.851 | 0.160 | 19 | 4117551 | missense variant | A/C;T | snv | 4 | |||
rs1057519806 | 0.882 | 0.200 | 19 | 4110583 | missense variant | T/C | snv | 3 | |||
rs727504382 | 0.925 | 0.200 | 19 | 4101105 | missense variant | C/T | snv | 2 | |||
rs727504370 | 0.925 | 0.200 | 19 | 4110558 | missense variant | T/C | snv | 2 | |||
rs267607230 | 0.925 | 0.160 | 19 | 4110576 | missense variant | G/A;C;T | snv | 2 | |||
rs121434497 | 0.925 | 0.160 | 19 | 4117552 | missense variant | A/C;T | snv | 2 | |||
rs121434499 | 0.925 | 0.160 | 19 | 4110559 | missense variant | A/G | snv | 2 | |||
rs1057519810 | 1.000 | 0.040 | 19 | 4117619 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
rs1057519809 | 1.000 | 0.040 | 19 | 4117586 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
rs1057519808 | 1.000 | 0.040 | 19 | 4117543 | missense variant | T/G | snv | 1 | |||
rs1057519807 | 1.000 | 0.040 | 19 | 4110586 | missense variant | A/T | snv | 1 | |||
rs730880517 | 1.000 | 0.160 | 19 | 4117541 | missense variant | T/C | snv | 1 | |||
rs1135401787 | 1.000 | 19 | 4117531 | missense variant | A/C;G | snv | 4.0E-06 | 1 | |||
rs387906800 | 1.000 | 19 | 4110564 | missense variant | C/T | snv | 1 |