Source: CLINVAR ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1085308045 | 0.807 | 0.160 | 10 | 87933128 | missense variant | C/G;T | snv | 8 | |||
rs1085308056 | 0.851 | 0.160 | 10 | 87957850 | splice region variant | C/G | snv | 8 | |||
rs1114167293 | 0.807 | 0.320 | 12 | 6944474 | splice acceptor variant | A/G | snv | 4.0E-06 | 7 | ||
rs121913293 | 0.732 | 0.360 | 10 | 87952142 | missense variant | C/A;T | snv | 18 | |||
rs140630794 | 0.925 | 0.040 | 21 | 36397429 | missense variant | A/C;G | snv | 1.3E-05; 4.2E-06 | 3 | ||
rs1555565492 | 0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins | 18 | |||
rs386834070 | 0.851 | 0.360 | 8 | 99134644 | stop gained | C/T | snv | 9 | |||
rs587776667 | 0.742 | 0.280 | 10 | 87931090 | splice donor variant | G/A;C;T | snv | 14 | |||
rs730882197 | 0.925 | 0.040 | 12 | 4525342 | frameshift variant | -/GTTT | delins | 4 |