Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs199473640 | 1.000 | 0.120 | 3 | 38550338 | missense variant | G/A | snv | 4.3E-05 | 2.1E-05 | 1 | |
rs199473639 | 1.000 | 0.080 | 3 | 38550469 | missense variant | A/C;G;T | snv | 1.6E-05; 4.1E-06; 4.1E-06 | 1 | ||
rs199473637 | 1.000 | 0.080 | 3 | 38550569 | missense variant | C/T | snv | 2.8E-05 | 1.4E-05 | 1 | |
rs199473636 | 1.000 | 0.080 | 3 | 38550791 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
rs199473635 | 1.000 | 3 | 38550896 | missense variant | G/A | snv | 1.6E-05 | 1.4E-05 | 1 | ||
rs199473634 | 0.925 | 0.120 | 3 | 38551036 | missense variant | G/A | snv | 4.0E-05 | 7.7E-05 | 2 | |
rs199473632 | 1.000 | 0.120 | 3 | 38551072 | missense variant | T/C | snv | 1 | |||
rs199473631 | 0.925 | 0.120 | 3 | 38551085 | missense variant | C/T | snv | 1 | |||
rs199473629 | 1.000 | 0.080 | 3 | 38551144 | missense variant | C/T | snv | 1 | |||
rs199473628 | 1.000 | 0.080 | 3 | 38551231 | missense variant | T/C | snv | 1 | |||
rs199473627 | 1.000 | 0.040 | 3 | 38551258 | missense variant | A/G | snv | 1 | |||
rs199473626 | 1.000 | 0.080 | 3 | 38551357 | missense variant | G/T | snv | 1 | |||
rs199473625 | 0.882 | 0.120 | 3 | 38551394 | missense variant | T/C | snv | 3.2E-05 | 7.0E-05 | 2 | |
rs199473624 | 1.000 | 0.080 | 3 | 38551447 | missense variant | C/T | snv | 1 | |||
rs199473623 | 0.882 | 0.120 | 3 | 38551486 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs199473622 | 1.000 | 0.120 | 3 | 38551546 | stop gained | G/A;C;T | snv | 1.2E-05 | 1 | ||
rs199473621 | 1.000 | 0.080 | 3 | 38554344 | missense variant | C/T | snv | 2.0E-05 | 2.1E-05 | 1 | |
rs199473620 | 1.000 | 0.080 | 3 | 38554372 | stop gained | C/A;T | snv | 1 | |||
rs199473619 | 1.000 | 0.120 | 3 | 38554412 | missense variant | C/G | snv | 4.0E-06 | 1 | ||
rs199473618 | 1.000 | 0.120 | 3 | 38554498 | missense variant | C/A;T | snv | 2.4E-05; 2.8E-04 | 1 | ||
rs199473617 | 1.000 | 0.080 | 3 | 38554530 | missense variant | A/G;T | snv | 1 | |||
rs199473616 | 1.000 | 0.120 | 3 | 38555731 | missense variant | C/A | snv | 4.0E-06 | 1 | ||
rs199473615 | 0.925 | 0.120 | 3 | 38555742 | missense variant | A/G | snv | 1 | |||
rs199473614 | 1.000 | 0.080 | 3 | 38556491 | missense variant | T/A | snv | 1 | |||
rs199473613 | 1.000 | 0.080 | 3 | 38556532 | missense variant | T/C | snv | 1 |