Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs80356779 | 0.776 | 0.320 | 11 | 68780662 | missense variant | G/A | snv | 3.2E-05 | 5.6E-05 | 10 | |
rs5030717 | 0.807 | 0.240 | 9 | 117711556 | intron variant | A/G | snv | 0.13 | 9 | ||
rs1800028 | 0.925 | 0.040 | 19 | 48703560 | stop gained | C/G;T | snv | 5.6E-04 | 3 | ||
rs10497394 | 0.925 | 0.040 | 2 | 173432931 | upstream gene variant | C/T | snv | 0.23 | 2 | ||
rs766490137 | 0.925 | 0.040 | 3 | 52458801 | missense variant | T/C | snv | 4.0E-06 | 2 |