Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs137853140 | 0.925 | 0.200 | 7 | 92235531 | missense variant | G/C | snv | 2 | |||
rs267607204 | 0.925 | 0.200 | 7 | 92234451 | stop gained | G/T | snv | 2 | |||
rs117153070 | 1.000 | 11 | 102834237 | intron variant | G/A | snv | 1.8E-02 | 1 | |||
rs137853139 | 1.000 | 7 | 92236488 | missense variant | T/C | snv | 1 | ||||
rs9823731 | 1.000 | 3 | 30641799 | intron variant | A/G | snv | 0.66 | 1 | |||
rs267607203 | 0.925 | 0.200 | 7 | 92222870 | stop gained | G/A;C | snv | 4.0E-06 | 2 | ||
rs10151332 | 1.000 | 14 | 99722950 | 3 prime UTR variant | C/T | snv | 3.2E-05; 0.48 | 0.41 | 1 |