Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1002481 | 0.882 | 0.080 | 6 | 111390819 | intron variant | T/A;G | snv | 3 | |||
rs10054203 | 0.882 | 0.080 | 5 | 1279849 | intron variant | G/A;C;T | snv | 3 | |||
rs10187911 | 0.882 | 0.080 | 2 | 50420809 | intron variant | C/A;G;T | snv | 3 | |||
rs1019340046 | 0.882 | 0.080 | 17 | 7674225 | missense variant | C/T | snv | 4 | |||
rs10213865 | 0.827 | 0.120 | 5 | 35857748 | intron variant | A/C;T | snv | 5 | |||
rs10254120 | 0.851 | 0.080 | 7 | 6005996 | missense variant | C/A;G;T | snv | 7.2E-02 | 5 | ||
rs1035938 | 0.776 | 0.120 | 19 | 47680514 | missense variant | C/G;T | snv | 0.29 | 8 | ||
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs1042711 | 0.827 | 0.120 | 5 | 148826785 | 5 prime UTR variant | C/A;G;T | snv | 4.2E-06; 0.68 | 5 | ||
rs1043973338 | 0.882 | 0.080 | 2 | 112830483 | missense variant | A/C | snv | 3 | |||
rs1043994 | 0.827 | 0.120 | 19 | 15192033 | synonymous variant | T/A;C | snv | 4.0E-06; 0.85 | 7 | ||
rs1044396 | 0.742 | 0.240 | 20 | 63349782 | missense variant | G/A;C | snv | 0.47; 6.1E-05 | 17 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs1046175 | 0.851 | 0.080 | 10 | 133391446 | stop gained | C/A;G;T | snv | 1.2E-05; 0.88 | 4 | ||
rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 43 | ||
rs104886026 | 0.851 | 0.080 | 7 | 55200333 | missense variant | G/A | snv | 4 | |||
rs10508266 | 0.882 | 0.080 | 10 | 3797822 | intergenic variant | G/A;T | snv | 3 | |||
rs1053566 | 0.882 | 0.080 | 19 | 7911079 | missense variant | C/T | snv | 3 | |||
rs1057519697 | 0.776 | 0.120 | 2 | 29220830 | missense variant | A/C | snv | 10 | |||
rs1057519729 | 0.827 | 0.080 | 15 | 66435113 | missense variant | A/C | snv | 5 | |||
rs1057519784 | 0.827 | 0.080 | 2 | 29220765 | missense variant | G/T | snv | 6 | |||
rs1057519847 | 0.570 | 0.560 | 7 | 55191821 | missense variant | CT/AG | mnv | 72 | |||
rs1057519848 | 0.570 | 0.560 | 7 | 55191822 | missense variant | TG/GT | mnv | 72 | |||
rs1057519857 | 0.882 | 0.080 | 17 | 39724772 | missense variant | T/C | snv | 3 | |||
rs1057519861 | 0.776 | 0.080 | 7 | 55181398 | missense variant | T/A | snv | 15 |