Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1060500142 | 1.000 | 0.080 | 1 | 237330939 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs1558698334 | 1.000 | 0.080 | 1 | 237369568 | missense variant | A/G | snv | 1 | |||
rs764772142 | 0.925 | 0.080 | 1 | 237377349 | missense variant | C/A;T | snv | 8.0E-06 | 2 | ||
rs397516539 | 1.000 | 0.080 | 1 | 237377365 | missense variant | G/A;T | snv | 1 | |||
rs1553426678 | 1.000 | 0.080 | 1 | 237377374 | missense variant | G/A | snv | 1 | |||
rs794728708 | 0.827 | 0.120 | 1 | 237377386 | missense variant | G/A;T | snv | 8 | |||
rs1415931588 | 1.000 | 0.080 | 1 | 237377426 | missense variant | A/T | snv | 2 | |||
rs1458500258 | 0.925 | 0.080 | 1 | 237388098 | missense variant | G/T | snv | 7.0E-06 | 3 | ||
rs1401116572 | 1.000 | 0.080 | 1 | 237441382 | missense variant | G/A | snv | 2 | |||
rs1553454821 | 1.000 | 0.080 | 1 | 237445428 | missense variant | G/A | snv | 1 | |||
rs759830423 | 1.000 | 0.080 | 1 | 237445447 | missense variant | C/T | snv | 2.0E-05 | 2.1E-05 | 1 | |
rs371121679 | 1.000 | 0.080 | 1 | 237445471 | missense variant | G/A;T | snv | 8.0E-06 | 1 | ||
rs1349176732 | 1.000 | 0.080 | 1 | 237445485 | missense variant | A/T | snv | 1 | |||
rs190140598 | 0.851 | 0.120 | 1 | 237445488 | missense variant | C/A;T | snv | 1.2E-05 | 4 | ||
rs794728721 | 0.925 | 0.080 | 1 | 237445489 | missense variant | G/A | snv | 3 | |||
rs121918602 | 0.925 | 0.120 | 1 | 237454396 | missense variant | T/C | snv | 3 | |||
rs376612295 | 1.000 | 0.080 | 1 | 237454494 | missense variant | C/G | snv | 1.0E-04 | 7.0E-05 | 1 | |
rs730880187 | 1.000 | 0.080 | 1 | 237492973 | missense variant | C/T | snv | 1 | |||
rs79457258 | 1.000 | 0.080 | 1 | 237550629 | missense variant | G/A;C | snv | 8.4E-05 | 1 | ||
rs730880191 | 1.000 | 0.080 | 1 | 237566623 | missense variant | G/A | snv | 8.0E-06; 4.0E-06 | 1 | ||
rs1553531703 | 1.000 | 0.080 | 1 | 237628052 | missense variant | G/A | snv | 1 | |||
rs1558103974 | 1.000 | 0.080 | 1 | 237633668 | missense variant | G/C | snv | 1 | |||
rs121918597 | 0.925 | 0.080 | 1 | 237634937 | missense variant | C/T | snv | 2 | |||
rs794728746 | 1.000 | 0.080 | 1 | 237638480 | missense variant | G/A;C | snv | 1 | |||
rs794728747 | 1.000 | 0.080 | 1 | 237639019 | missense variant | G/T | snv | 1 |