Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13768 | 1.000 | 0.120 | 1 | 156138660 | missense variant | G/A;T | snv | 2.4E-05 | 1 | ||
rs1553265999 | 1.000 | 0.120 | 1 | 156136925 | missense variant | A/C | snv | 1 | |||
rs267607539 | 1.000 | 0.120 | 1 | 156137237 | splice region variant | G/A;C | snv | 1 | |||
rs267607540 | 1.000 | 0.120 | 1 | 156134509 | inframe deletion | GAA/- | delins | 1 | |||
rs267607614 | 1.000 | 0.120 | 1 | 156115016 | missense variant | A/G | snv | 1 | |||
rs267607629 | 1.000 | 0.120 | 1 | 156134507 | missense variant | C/G | snv | 1 | |||
rs267607630 | 1.000 | 0.120 | 1 | 156134967 | missense variant | T/C | snv | 1 | |||
rs267607633 | 1.000 | 0.120 | 1 | 156135259 | missense variant | T/C | snv | 1 | |||
rs267607638 | 1.000 | 0.120 | 1 | 156136417 | missense variant | T/C | snv | 1 | |||
rs267607641 | 1.000 | 0.120 | 1 | 156135188 | missense variant | T/C | snv | 1 | |||
rs267607642 | 1.000 | 0.120 | 1 | 156136921 | missense variant | G/T | snv | 8.0E-06 | 1 | ||
rs267607643 | 1.000 | 0.120 | 1 | 156134455 | missense variant | GG/CC | mnv | 1 | |||
rs56694480 | 1.000 | 0.120 | 1 | 156115021 | missense variant | C/G | snv | 1 | |||
rs56699480 | 1.000 | 0.120 | 1 | 156137017 | stop gained | C/T | snv | 1 | |||
rs57048196 | 1.000 | 0.120 | 1 | 156134965 | missense variant | A/G | snv | 1 | |||
rs57394692 | 1.000 | 0.120 | 1 | 156136946 | missense variant | T/C | snv | 1 | |||
rs57793737 | 1.000 | 0.120 | 1 | 156115106 | missense variant | T/A;C;G | snv | 1 | |||
rs58105277 | 1.000 | 0.120 | 1 | 156135971 | missense variant | G/A | snv | 2.8E-05 | 1 | ||
rs58541611 | 1.000 | 0.120 | 1 | 156136393 | missense variant | A/G;T | snv | 1 | |||
rs59931416 | 1.000 | 0.120 | 1 | 156115066 | missense variant | C/A;T | snv | 1 | |||
rs60446065 | 1.000 | 0.120 | 1 | 156115045 | missense variant | G/A | snv | 1 | |||
rs60992550 | 1.000 | 0.120 | 1 | 156136423 | missense variant | A/T | snv | 1 | |||
rs61177390 | 1.000 | 0.120 | 1 | 156135992 | missense variant | G/A | snv | 3.6E-05 | 2.8E-05 | 1 | |
rs61235244 | 1.000 | 0.120 | 1 | 156136424 | missense variant | C/A | snv | 1 | |||
rs61527854 | 1.000 | 0.120 | 1 | 156135283 | missense variant | T/C | snv | 1 |