Source: UNIPROT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104894827 | 1.000 | 0.160 | X | 101398033 | missense variant | G/A | snv | 1 | |||
rs104894828 | 0.882 | 0.160 | X | 101398467 | missense variant | C/A;T | snv | 1 | |||
rs104894830 | 0.925 | 0.160 | X | 101398483 | missense variant | T/C | snv | 1 | |||
rs104894831 | 1.000 | 0.160 | X | 101407786 | missense variant | G/A | snv | 1 | |||
rs104894832 | 1.000 | 0.160 | X | 101398387 | missense variant | C/G;T | snv | 1 | |||
rs104894834 | 1.000 | 0.160 | X | 101403846 | missense variant | G/A | snv | 1 | |||
rs104894835 | 1.000 | 0.160 | X | 101407803 | missense variant | T/C | snv | 1 | |||
rs104894836 | 1.000 | 0.160 | X | 101407738 | missense variant | A/C | snv | 1 | |||
rs104894837 | 1.000 | 0.160 | X | 101401743 | missense variant | G/A | snv | 1 | |||
rs104894838 | 1.000 | 0.160 | X | 101400699 | missense variant | A/C | snv | 1 | |||
rs104894840 | 1.000 | 0.160 | X | 101398906 | missense variant | C/G;T | snv | 1 | |||
rs104894846 | 0.925 | 0.160 | X | 101398481 | missense variant | C/T | snv | 1 | |||
rs104894847 | 0.925 | 0.160 | X | 101407846 | missense variant | C/G | 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 | |||
rs1057521047 | 1.000 | 0.160 | X | 101407750 | missense variant | A/G | snv | 1 | |||
rs113173389 | 1.000 | 0.160 | X | 101403899 | missense variant | C/T | snv | 1 | |||
rs1555984869 | 1.000 | 0.160 | X | 101398081 | missense variant | A/G | snv | 1 | |||
rs1555985175 | 1.000 | 0.160 | X | 101398916 | missense variant | T/C | snv | 1 | |||
rs1555985829 | 1.000 | 0.160 | X | 101401736 | missense variant | C/A;T | snv | 1 | |||
rs28935195 | 0.925 | 0.200 | X | 101401713 | missense variant | C/T | snv | 1 | |||
rs28935196 | 1.000 | 0.160 | X | 101401695 | missense variant | A/G | snv | 1 | |||
rs28935485 | 0.925 | 0.160 | X | 101398534 | missense variant | G/C | snv | 1 | |||
rs28935486 | 1.000 | 0.160 | X | 101398795 | missense variant | T/A | snv | 1 | |||
rs28935487 | 1.000 | 0.160 | X | 101398789 | missense variant | T/A;G | snv | 1 |