Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121434358 | 0.882 | 0.240 | 19 | 8605638 | missense variant | C/T | snv | 3.2E-05 | 2.1E-04 | 3 | |
rs137854856 | 0.882 | 0.240 | 14 | 74508727 | missense variant | C/G;T | snv | 4.0E-06 | 3 | ||
rs71530910 | 0.882 | 0.360 | 4 | 6301680 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 3 | |
rs769194347 | 0.925 | 0.240 | 1 | 150556630 | missense variant | G/A | snv | 1.2E-05 | 2 | ||
rs1441536824 | 0.925 | 0.240 | 15 | 48513551 | missense variant | C/T | snv | 2.0E-05 | 7.0E-06 | 2 | |
rs144453318 | 1.000 | 0.120 | 4 | 89953260 | missense variant | A/G | snv | 1 |