Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs730882020 | 0.925 | 0.160 | 3 | 10149798 | frameshift variant | A/-;AA | delins | 2 | |||
rs1553619461 | 1.000 | 0.120 | 3 | 10142160 | missense variant | A/C | snv | 1 | |||
rs869025643 | 1.000 | 0.120 | 3 | 10146547 | missense variant | A/C | snv | 1 | |||
rs786202787 | 1.000 | 0.120 | 3 | 10142085 | missense variant | A/C;G | snv | 2 | |||
rs864321643 | 0.925 | 0.160 | 3 | 10142140 | missense variant | A/C;G | snv | 2 | |||
rs1347416980 | 1.000 | 0.120 | 3 | 10146568 | missense variant | A/C;G | snv | 4.0E-06 | 1 | ||
rs5030812 | 1.000 | 0.120 | 3 | 10146517 | missense variant | A/C;G | snv | 1 | |||
rs869025621 | 0.882 | 0.240 | 3 | 10142079 | missense variant | A/C;G;T | snv | 4 | |||
rs5030804 | 0.925 | 0.160 | 3 | 10142080 | missense variant | A/C;G;T | snv | 3 | |||
rs143985153 | 1.000 | 0.120 | 3 | 10142116 | missense variant | A/C;G;T | snv | 1 | |||
rs397516441 | 0.882 | 0.200 | 3 | 10149790 | missense variant | A/G | snv | 4 | |||
rs869025648 | 0.851 | 0.240 | 3 | 10146587 | synonymous variant | A/G | snv | 4 | |||
rs1271401320 | 1.000 | 0.120 | 9 | 21440749 | missense variant | A/G | snv | 3 | |||
rs267607170 | 0.882 | 0.200 | 3 | 10149814 | missense variant | A/G | snv | 3 | |||
rs1559428091 | 0.925 | 0.160 | 3 | 10146543 | missense variant | A/G | snv | 2 | |||
rs5030832 | 0.925 | 0.160 | 3 | 10146535 | missense variant | A/G | snv | 2 | |||
rs1553619963 | 1.000 | 0.120 | 3 | 10146565 | missense variant | A/G | snv | 1 | |||
rs377715747 | 1.000 | 0.120 | 3 | 10149861 | missense variant | A/G | snv | 8.0E-06 | 1.4E-05 | 1 | |
rs869025637 | 1.000 | 0.120 | 3 | 10146512 | splice acceptor variant | A/G | snv | 1 | |||
rs869025642 | 1.000 | 0.120 | 3 | 10146531 | missense variant | A/G | snv | 1 | |||
rs77724903 | 0.672 | 0.280 | 10 | 43118460 | missense variant | A/G;T | snv | 4.0E-06; 2.1E-03 | 23 | ||
rs193922613 | 0.925 | 0.160 | 3 | 10149847 | missense variant | A/G;T | snv | 3 | |||
rs5030816 | 0.925 | 0.160 | 3 | 10149785 | splice acceptor variant | A/G;T | snv | 3 | |||
rs1559426203 | 0.925 | 0.160 | 3 | 10142178 | missense variant | A/G;T | snv | 2 | |||
rs1559430011 | 1.000 | 0.120 | 3 | 10149965 | stop lost | A/G;T | snv | 1 |