Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs147952620 | 0.925 | 0.160 | 7 | 107690199 | missense variant | C/T | snv | 1.6E-05 | 3 | ||
rs1554360358 | 0.925 | 0.160 | 7 | 107698076 | missense variant | A/C | snv | 3 | |||
rs201660407 | 0.925 | 0.160 | 7 | 107690236 | missense variant | A/C;G | snv | 8.0E-06; 1.2E-05 | 3 | ||
rs747076316 | 0.925 | 0.160 | 7 | 107694622 | stop gained | C/A;G;T | snv | 2.0E-05 | 2.1E-05 | 3 | |
rs752807925 | 0.925 | 0.160 | 7 | 107704382 | stop gained | C/T | snv | 1.3E-05 | 3 | ||
rs763006761 | 0.925 | 0.160 | 7 | 107700135 | missense variant | A/G | snv | 1.6E-05 | 3 | ||
rs786204474 | 0.925 | 0.160 | 7 | 107689130 | missense variant | C/T | snv | 7.0E-06 | 3 | ||
rs786204601 | 0.925 | 0.160 | 7 | 107696014 | frameshift variant | T/- | delins | 3 | |||
rs786204739 | 0.925 | 0.160 | 7 | 107698083 | missense variant | T/G | snv | 3 | |||
rs912147281 | 0.925 | 0.160 | 7 | 107683356 | splice donor variant | T/C | snv | 8.0E-06 | 1.4E-05 | 3 | |
rs1057516953 | 0.925 | 0.160 | 7 | 107663412 | missense variant | C/T | snv | 4.0E-06 | 3 | ||
rs786204581 | 0.925 | 0.160 | 7 | 107663366 | stop gained | C/T | snv | 3 | |||
rs1060499808 | 0.925 | 0.160 | 7 | 107704344 | missense variant | T/C | snv | 8.9E-06 | 2 | ||
rs111033257 | 0.925 | 0.160 | 7 | 107700162 | missense variant | G/A | snv | 1.4E-05 | 2 | ||
rs111033303 | 0.925 | 0.160 | 7 | 107674970 | missense variant | G/T | snv | 3.0E-04 | 3.8E-04 | 2 | |
rs111033308 | 0.925 | 0.160 | 7 | 107695984 | missense variant | G/A;C | snv | 2.0E-05 | 6.3E-05 | 2 | |
rs121908365 | 0.925 | 0.160 | 7 | 107672230 | missense variant | T/A;C | snv | 2 | |||
rs145254330 | 0.925 | 0.160 | 7 | 107672182 | missense variant | C/T | snv | 3.3E-04 | 1.7E-04 | 2 | |
rs146281367 | 0.925 | 0.160 | 7 | 107683537 | missense variant | G/A;C;T | snv | 4.0E-06; 8.0E-06 | 2 | ||
rs1554354787 | 0.925 | 0.160 | 7 | 107674188 | missense variant | T/C | snv | 2 | |||
rs1554359670 | 0.925 | 0.160 | 7 | 107694650 | missense variant | C/A | snv | 2 | |||
rs397516413 | 0.925 | 0.160 | 7 | 107690171 | frameshift variant | T/- | delins | 7.0E-06 | 2 | ||
rs397516414 | 0.925 | 0.160 | 7 | 107690178 | missense variant | G/A | snv | 2 | |||
rs431905486 | 0.925 | 0.160 | 7 | 107683531 | frameshift variant | -/A | delins | 2 | |||
rs542620119 | 0.925 | 0.160 | 7 | 107674302 | missense variant | G/C | snv | 9.1E-05 | 3.5E-05 | 2 |