Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs267606805 | 0.851 | 0.240 | 8 | 38414173 | missense variant | G/T | snv | 5 | |||
rs267606806 | 0.851 | 0.240 | 8 | 38414166 | missense variant | G/A;C | snv | 1.2E-05 | 5 | ||
rs3811046 | 0.851 | 0.160 | 2 | 112913801 | missense variant | G/A;T | snv | 4.0E-06; 0.71 | 5 | ||
rs121909636 | 0.827 | 0.240 | 8 | 38414569 | stop gained | G/A | snv | 7 | |||
rs121909635 | 0.827 | 0.240 | 8 | 38426158 | missense variant | C/T | snv | 6 | |||
rs121908119 | 0.763 | 0.200 | 2 | 218882368 | stop gained | C/A | snv | 6.2E-04 | 8.5E-04 | 10 | |
rs1800796 | 0.555 | 0.760 | 7 | 22726627 | non coding transcript exon variant | G/C | snv | 9.9E-02 | 74 | ||
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 |