Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1476413 | 0.790 | 0.360 | 1 | 11792243 | intron variant | C/G;T | snv | 4.0E-06; 0.26 | 0.23 | 10 | |
rs165656 | 0.925 | 0.200 | 22 | 19961340 | intron variant | G/A;C;T | snv | 5 | |||
rs723744 | 0.925 | 0.200 | 18 | 31592513 | intron variant | G/T | snv | 0.38 | 3 | ||
rs752306 | 0.925 | 0.200 | 11 | 637622 | intron variant | C/T | snv | 6.4E-02 | 4.8E-02 | 3 | |
rs225010 | 1.000 | 0.200 | 14 | 80205936 | intron variant | C/T | snv | 0.51 | 2 | ||
rs225012 | 1.000 | 0.200 | 14 | 80204392 | intron variant | A/C;G | snv | 0.51 | 2 | ||
rs6511901 | 1.000 | 0.200 | 19 | 13916839 | intron variant | C/T | snv | 0.39 | 2 | ||
rs6530893 | 1.000 | 0.200 | 8 | 15671068 | intron variant | T/C | snv | 0.14 | 2 | ||
rs6994908 | 1.000 | 0.200 | 8 | 15674943 | intron variant | T/C | snv | 0.32 | 2 | ||
rs255012 | 1.000 | 0.200 | 7 | 41189487 | regulatory region variant | T/A;C | snv | 2 | |||
rs724159949 | 0.827 | 0.240 | 21 | 37486563 | stop gained | C/T | snv | 15 | |||
rs61748421 | 0.807 | 0.200 | X | 154031326 | stop gained | G/A;T | snv | 9 | |||
rs122445108 | 0.807 | 0.320 | X | 77717155 | stop gained | G/A | snv | 7 | |||
rs121965020 | 0.827 | 0.280 | 4 | 987858 | stop gained | C/T | snv | 4.7E-04 | 6.1E-04 | 6 | |
rs45517305 | 0.851 | 0.240 | 16 | 2081646 | stop gained | C/A;T | snv | 5 | |||
rs121918368 | 0.925 | 0.200 | 3 | 3150939 | stop gained | G/A | snv | 8.0E-06 | 7.0E-06 | 3 | |
rs121918523 | 0.925 | 0.200 | X | 54016662 | stop gained | T/A | snv | 3 | |||
rs122468181 | 0.925 | 0.200 | X | 119837771 | stop gained | G/A;T | snv | 3 | |||
rs1427146168 | 1.000 | 0.200 | 9 | 131140671 | stop gained | C/T | snv | 2 | |||
rs794729221 | 0.925 | 0.240 | 1 | 42929736 | stop gained | G/A | snv | 2 | |||
rs878853149 | 0.925 | 0.240 | 18 | 55350388 | stop gained | G/A | snv | 2 | |||
rs878853144 | 1.000 | 0.200 | X | 53239213 | stop gained | G/A | snv | 1 | |||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs1801131 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 93 |