Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4647924 | 0.600 | 0.520 | 4 | 1801844 | missense variant | C/A;G;T | snv | 4.2E-06; 4.2E-06 | 49 | ||
rs121913482 | 0.630 | 0.680 | 4 | 1801837 | missense variant | C/T | snv | 45 | |||
rs121913483 | 0.649 | 0.560 | 4 | 1801841 | missense variant | C/A;G;T | snv | 4.2E-06; 1.3E-05 | 31 | ||
rs121913105 | 0.653 | 0.600 | 4 | 1806163 | missense variant | A/C;T | snv | 30 | |||
rs28933068 | 0.645 | 0.560 | 4 | 1805644 | missense variant | C/A;G;T | snv | 1.6E-05 | 30 | ||
rs28931614 | 0.672 | 0.520 | 4 | 1804392 | missense variant | G/A;C | snv | 21 | |||
rs28931615 | 0.732 | 0.240 | 4 | 1804426 | missense variant | C/A;T | snv | 13 | |||
rs587781858 | 0.742 | 0.360 | 17 | 7669671 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06 | 12 | ||
rs121913479 | 0.763 | 0.280 | 4 | 1804362 | missense variant | G/A;T | snv | 4.0E-06 | 10 | ||
rs121913116 | 0.763 | 0.360 | 4 | 1799395 | missense variant | C/T | snv | 9 | |||
rs1211533350 | 0.827 | 0.120 | 4 | 1805638 | synonymous variant | C/A | snv | 4.0E-06 | 7.0E-06 | 5 | |
rs121913114 | 0.925 | 0.120 | 4 | 1801930 | missense variant | A/G;T | snv | 4.0E-06 | 2 | ||
rs75790268 | 0.925 | 0.120 | 4 | 1804377 | missense variant | G/T | snv | 2 | |||
rs770873375 | 0.925 | 0.080 | 7 | 50612776 | missense variant | T/C | snv | 2.4E-05 | 2 | ||
rs144478519 | 0.925 | 0.120 | 2 | 113062547 | stop gained | C/A;T | snv | 4.0E-06; 2.9E-03 | 2 | ||
rs756254503 | 0.925 | 0.120 | 5 | 151669740 | missense variant | G/C | snv | 4.0E-06 | 2 | ||
rs12822 | 1.000 | 0.080 | 6 | 32977925 | stop gained | G/A;T | snv | 1.5E-05 | 1 | ||
rs1397150560 | 1.000 | 0.080 | 6 | 32978186 | missense variant | A/G | snv | 4.1E-06 | 1 | ||
rs751731391 | 1.000 | 0.080 | 10 | 121500901 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs267608572 | 1.000 | 0.080 | X | 154030690 | missense variant | C/T | snv | 3.5E-04 | 2.2E-04 | 1 | |
rs776165919 | 1.000 | 0.080 | 6 | 144437643 | missense variant | G/A | snv | 8.8E-05 | 1 |