Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs869025672 | 0.925 | 0.320 | 8 | 38414872 | missense variant | A/C;G | snv | 8.0E-06 | 1 | ||
rs121909633 | 1.000 | 0.080 | 8 | 38424546 | missense variant | A/G | snv | 2.9E-04 | 4.1E-04 | 1 | |
rs121909634 | 1.000 | 0.080 | 8 | 38419676 | missense variant | A/G | snv | 1 | |||
rs121909638 | 0.882 | 0.280 | 8 | 38421853 | missense variant | A/G | snv | 1 | |||
rs397515481 | 1.000 | 0.280 | 8 | 38428048 | missense variant | A/G | snv | 1 | |||
rs869025669 | 1.000 | 0.280 | 8 | 38427970 | missense variant | A/G | snv | 1 | |||
rs121909630 | 0.925 | 0.160 | 8 | 38428043 | missense variant | C/A | snv | 1 | |||
rs398122946 | 1.000 | 0.280 | 8 | 38414889 | missense variant | C/A | snv | 1 | |||
rs121909637 | 0.882 | 0.240 | 8 | 38418249 | missense variant | C/A;T | snv | 1.2E-05; 2.0E-05 | 1 | ||
rs121909644 | 0.925 | 0.160 | 8 | 38413795 | missense variant | C/A;T | snv | 1 | |||
rs140254426 | 1.000 | 0.160 | 8 | 38429832 | missense variant | C/A;T | snv | 8.0E-06 | 1 | ||
rs760884357 | 1.000 | 0.160 | 8 | 38457435 | missense variant | C/G | snv | 4.0E-06 | 1 | ||
rs869025671 | 1.000 | 0.280 | 8 | 38414876 | missense variant | C/G | snv | 1 | |||
rs121909645 | 0.925 | 0.240 | 8 | 38424696 | missense variant | C/G;T | snv | 1 | |||
rs869025670 | 1.000 | 0.280 | 8 | 38417954 | missense variant | C/G;T | snv | 1 | |||
rs886037634 | 0.925 | 0.160 | 8 | 38421836 | missense variant | C/T | snv | 1 | |||
rs121909635 | 0.827 | 0.240 | 8 | 38426158 | missense variant | C/T | snv | 1 | |||
rs781328162 | 0.925 | 0.160 | 8 | 38413714 | missense variant | C/T | snv | 2.0E-05 | 3.5E-05 | 1 | |
rs397515446 | 0.925 | 0.160 | 8 | 38414599 | missense variant | C/T | snv | 1 | |||
rs121909640 | 0.925 | 0.160 | 8 | 38429898 | missense variant | C/T | snv | 1 | |||
rs749758370 | 1.000 | 0.160 | 8 | 38417411 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
rs55642501 | 1.000 | 0.160 | 8 | 38429736 | missense variant | C/T | snv | 4.2E-04 | 1.7E-04 | 1 | |
rs121909629 | 0.882 | 0.200 | 8 | 38415905 | missense variant | C/T | snv | 1 | |||
rs768957161 | 1.000 | 0.160 | 8 | 38414231 | missense variant | C/T | snv | 2.8E-05 | 2.8E-05 | 1 | |
rs1131691929 | 1.000 | 0.160 | 8 | 38424628 | missense variant | C/T | snv | 1 |