Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs387907252 | 0.882 | 0.160 | 10 | 117134559 | missense variant | G/T | snv | 3 | |||
rs1329285216 | 0.925 | 0.080 | 10 | 93593997 | missense variant | A/T | snv | 2 | |||
rs755377651 | 0.925 | 0.080 | 1 | 47416625 | missense variant | C/G;T | snv | 4.0E-06; 4.0E-06 | 2 | ||
rs80358194 | 0.925 | 0.080 | 1 | 47417035 | stop gained | C/A | snv | 1.6E-04 | 2 | ||
rs377669670 | 0.925 | 0.080 | 1 | 47416547 | missense variant | G/A | snv | 3.6E-05 | 6.4E-05 | 2 | |
rs1554985722 | 0.925 | 0.200 | 11 | 31802714 | missense variant | C/G | snv | 2 | |||
rs387907095 | 0.925 | 0.080 | 2 | 232523492 | missense variant | G/C | snv | 2 | |||
rs587777690 | 0.925 | 0.080 | 17 | 32940889 | missense variant | G/C;T | snv | 4.0E-06 | 2 | ||
rs869312733 | 0.925 | 0.080 | 17 | 32940899 | missense variant | A/C | snv | 2 | |||
rs552445199 | 0.925 | 0.080 | 18 | 68711389 | missense variant | C/T | snv | 2.9E-05 | 1.4E-05 | 2 | |
rs755799430 | 0.925 | 0.080 | 14 | 74259689 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 2 | |
rs1569119395 | 0.925 | 0.120 | 22 | 45949926 | stop gained | G/A | snv | 2 | |||
rs374823079 | 1.000 | 0.080 | 11 | 119341673 | missense variant | G/A | snv | 8.5E-05 | 3.5E-05 | 1 | |
rs869025268 | 1.000 | 0.080 | 14 | 74239626 | frameshift variant | -/G | delins | 1.3E-05 | 1 | ||
rs1475762618 | 1.000 | 0.080 | 22 | 45923167 | missense variant | G/A | snv | 1 |