Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs377767406 | 0.776 | 0.120 | 10 | 43114491 | missense variant | G/A;T | snv | 4.0E-05; 4.0E-06 | 9 | ||
rs377767398 | 0.807 | 0.280 | 10 | 43113628 | missense variant | GC/AT;CT;TT | mnv | 8 | |||
rs77503355 | 0.776 | 0.160 | 10 | 43113655 | missense variant | G/A;C;T | snv | 8 | |||
rs77558292 | 0.776 | 0.160 | 10 | 43113621 | missense variant | T/A;C;G | snv | 8 | |||
rs146646971 | 0.807 | 0.120 | 10 | 43114598 | missense variant | G/C;T | snv | 2.4E-05 | 7 | ||
rs377767429 | 0.790 | 0.120 | 10 | 43120120 | missense variant | GC/TT | mnv | 7 | |||
rs75030001 | 0.807 | 0.160 | 10 | 43118458 | missense variant | G/C;T | snv | 4.0E-06; 2.0E-05 | 7 | ||
rs1555166368 | 0.851 | 0.120 | 11 | 64809738 | frameshift variant | GA/- | del | 6 | |||
rs121913308 | 0.827 | 0.120 | 10 | 43114492 | missense variant | A/C;G;T | snv | 6 | |||
rs143795581 | 0.851 | 0.120 | 10 | 43114596 | missense variant | A/C;G | snv | 8.0E-06 | 5 | ||
rs377767391 | 0.827 | 0.160 | 10 | 43113627 | missense variant | T/A;C;G | snv | 5 | |||
rs377767442 | 0.827 | 0.160 | 10 | 43121967 | missense variant | A/G | snv | 5 | |||
rs1188536960 | 0.882 | 0.120 | 15 | 45043305 | missense variant | A/G | snv | 5 | |||
rs121913306 | 0.851 | 0.120 | 10 | 43120119 | missense variant | AGC/TTT | mnv | 4 | |||
rs146838520 | 0.851 | 0.120 | 10 | 43120129 | missense variant | C/T | snv | 4.0E-06 | 2.8E-05 | 4 | |
rs1800863 | 0.851 | 0.160 | 10 | 43120185 | synonymous variant | C/A;G | snv | 1.6E-05; 0.21 | 4 | ||
rs34682185 | 0.851 | 0.120 | 10 | 43106382 | missense variant | G/A | snv | 6.3E-04 | 2.2E-04 | 4 | |
rs377767395 | 0.882 | 0.120 | 10 | 43113613 | missense variant | A/G | snv | 4 | |||
rs781609053 | 0.925 | 0.120 | 7 | 55200379 | missense variant | T/C | snv | 1.2E-05 | 3 | ||
rs148935214 | 0.882 | 0.240 | 10 | 43114546 | missense variant | C/T | snv | 3.2E-04 | 3.8E-04 | 3 | |
rs377767427 | 0.882 | 0.120 | 10 | 43120114 | missense variant | C/G | snv | 4.0E-06 | 3 | ||
rs78347871 | 0.882 | 0.120 | 10 | 43121950 | missense variant | G/A;C;T | snv | 8.0E-06; 2.0E-05 | 3 | ||
rs864622088 | 0.925 | 0.080 | 9 | 95459774 | missense variant | G/T | snv | 4.0E-06 | 2 | ||
rs2075912 | 0.925 | 0.160 | 10 | 43126769 | 3 prime UTR variant | T/C | snv | 0.79 | 0.84 | 2 | |
rs2565200 | 0.925 | 0.160 | 10 | 43127485 | 3 prime UTR variant | T/A;C | snv | 2 |