Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121908334 | 0.925 | 0.080 | 10 | 86687218 | missense variant | C/T | snv | 4.0E-06 | 3 | ||
rs121908336 | 1.000 | 0.040 | 10 | 86706669 | missense variant | C/G;T | snv | 4.0E-06; 2.8E-04 | 1 | ||
rs45487699 | 1.000 | 0.040 | 10 | 86681680 | missense variant | C/T | snv | 6.5E-04 | 5.0E-04 | 1 | |
rs121908337 | 1.000 | 0.040 | 10 | 86681731 | missense variant | C/T | snv | 1.6E-05 | 7.0E-06 | 1 | |
rs775180716 | 1.000 | 0.080 | 10 | 86692544 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs121908333 | 1.000 | 10 | 86687163 | missense variant | G/A | snv | 1 |