Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121909627 | 0.776 | 0.200 | 8 | 38424690 | missense variant | G/C | snv | 4.0E-06 | 2 | ||
rs1085307879 | 1.000 | 0.160 | 8 | 38414183 | missense variant | T/C | snv | 1 | |||
rs1131691929 | 1.000 | 0.160 | 8 | 38424628 | missense variant | C/T | snv | 1 | |||
rs121909628 | 0.925 | 0.160 | 8 | 38414892 | stop gained | G/A;C | snv | 1 | |||
rs121909629 | 0.882 | 0.200 | 8 | 38415905 | missense variant | C/T | snv | 1 | |||
rs121909630 | 0.925 | 0.160 | 8 | 38428043 | missense variant | C/A | snv | 1 | |||
rs121909635 | 0.827 | 0.240 | 8 | 38426158 | missense variant | C/T | snv | 1 | |||
rs121909637 | 0.882 | 0.240 | 8 | 38418249 | missense variant | C/A;T | snv | 1.2E-05; 2.0E-05 | 1 | ||
rs121909638 | 0.882 | 0.280 | 8 | 38421853 | missense variant | A/G | snv | 1 | |||
rs121909640 | 0.925 | 0.160 | 8 | 38429898 | missense variant | C/T | snv | 1 | |||
rs121909641 | 0.763 | 0.520 | 8 | 38419720 | missense variant | G/A | snv | 1 | |||
rs121909642 | 0.925 | 0.160 | 8 | 38414174 | missense variant | G/A | snv | 1 | |||
rs121909644 | 0.925 | 0.160 | 8 | 38413795 | missense variant | C/A;T | snv | 1 | |||
rs121909645 | 0.925 | 0.240 | 8 | 38424696 | missense variant | C/G;T | snv | 1 | |||
rs140254426 | 1.000 | 0.160 | 8 | 38429832 | missense variant | C/A;T | snv | 8.0E-06 | 1 | ||
rs1554570706 | 0.925 | 0.200 | 8 | 38429808 | missense variant | G/A | snv | 1 | |||
rs397515444 | 0.925 | 0.160 | 8 | 38417975 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
rs397515445 | 0.807 | 0.280 | 8 | 38414263 | missense variant | T/C | snv | 1 | |||
rs397515446 | 0.925 | 0.160 | 8 | 38414599 | missense variant | C/T | snv | 1 | |||
rs55642501 | 1.000 | 0.160 | 8 | 38429736 | missense variant | C/T | snv | 4.2E-04 | 1.7E-04 | 1 | |
rs727505369 | 0.925 | 0.160 | 8 | 38424624 | missense variant | T/C | snv | 1 | |||
rs727505373 | 0.925 | 0.160 | 8 | 38429744 | missense variant | T/C | snv | 1 | |||
rs747842199 | 1.000 | 0.160 | 8 | 38429694 | missense variant | C/T | snv | 2.8E-05 | 1.4E-05 | 1 | |
rs749758370 | 1.000 | 0.160 | 8 | 38417411 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
rs760884357 | 1.000 | 0.160 | 8 | 38457435 | missense variant | C/G | snv | 4.0E-06 | 1 |