Source: UNIPROT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104894837 | 1.000 | 0.160 | X | 101401743 | missense variant | G/A | snv | 1 | |||
rs104894840 | 1.000 | 0.160 | X | 101398906 | missense variant | C/G;T | snv | 1 | |||
rs104894845 | 0.807 | 0.160 | X | 101401752 | missense variant | C/G;T | snv | 5.5E-04 | 1 | ||
rs104894846 | 0.925 | 0.160 | X | 101398481 | missense variant | C/T | snv | 1 | |||
rs104894848 | 1.000 | 0.160 | X | 101407710 | missense variant | C/G | snv | 1 | |||
rs104894852 | 0.925 | 0.200 | X | 101397871 | missense variant | T/C | snv | 1 | |||
rs1555985829 | 1.000 | 0.160 | X | 101401736 | missense variant | C/A;T | snv | 1 | |||
rs28935197 | 0.776 | 0.280 | X | 101398942 | missense variant | T/C | snv | 5.5E-06 | 1 | ||
rs28935485 | 0.925 | 0.160 | X | 101398534 | missense variant | G/C | snv | 1 | |||
rs28935488 | 1.000 | 0.160 | X | 101398563 | missense variant | A/C;G;T | snv | 1 | |||
rs28935489 | 1.000 | 0.160 | X | 101398479 | missense variant | G/A;C | snv | 1 | |||
rs28935491 | 1.000 | 0.160 | X | 101398390 | stop gained | G/A;T | snv | 1 | |||
rs28935492 | 1.000 | 0.160 | X | 101398386 | missense variant | C/G | snv | 1 | |||
rs397515873 | 1.000 | 0.160 | X | 101398862 | missense variant | T/A;C | snv | 1 | |||
rs397515874 | 1.000 | 0.160 | X | 101398857 | missense variant | C/G;T | snv | 5.5E-06 | 1 | ||
rs398123201 | 1.000 | 0.160 | X | 101407779 | missense variant | A/G | snv | 1 | |||
rs727503950 | 1.000 | 0.160 | X | 101400712 | missense variant | A/G | snv | 1.1E-05 | 1.9E-05 | 1 | |
rs727504348 | 0.925 | 0.160 | X | 101397982 | missense variant | C/T | snv | 1 | |||
rs730880439 | 1.000 | 0.160 | X | 101398408 | missense variant | G/C | snv | 1 | |||
rs730880451 | 1.000 | 0.160 | X | 101398785 | missense variant | C/T | snv | 1 | |||
rs782598150 | 1.000 | 0.160 | X | 101398021 | missense variant | C/A;G | snv | 5.5E-06 | 1 | ||
rs797044746 | 1.000 | 0.160 | X | 101398882 | missense variant | G/C | snv | 1 | |||
rs797044774 | 1.000 | 0.160 | X | 101398027 | missense variant | C/T | snv | 1 | |||
rs869312135 | 1.000 | 0.160 | X | 101407842 | missense variant | A/G | snv | 1 | |||
rs869312138 | 1.000 | 0.160 | X | 101407797 | missense variant | A/C | snv | 1 |