Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
rs2228570 | 0.521 | 0.760 | 12 | 47879112 | start lost | A/C;G;T | snv | 0.63 | 99 | ||
rs3775291 | 0.602 | 0.640 | 4 | 186082920 | missense variant | C/G;T | snv | 1.2E-04; 0.28 | 51 | ||
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 46 | ||
rs8192284 | 0.724 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 19 | |||
rs10774671 | 0.732 | 0.480 | 12 | 112919388 | splice acceptor variant | G/A;C | snv | 0.67 | 14 | ||
rs2072136 | 0.851 | 0.120 | 12 | 112961114 | synonymous variant | G/A;C | snv | 0.31; 4.0E-06 | 6 | ||
rs6141 | 0.925 | 0.080 | 3 | 184372478 | 3 prime UTR variant | C/G;T | snv | 4.0E-06; 0.56 | 4 | ||
rs669260 | 0.851 | 0.080 | 9 | 32503442 | intron variant | T/A;C | snv | 4 | |||
rs1131454 | 0.882 | 0.040 | 12 | 112911065 | missense variant | G/A;C | snv | 0.57 | 3 | ||
rs1447043692 | 0.925 | 0.040 | 10 | 98641918 | missense variant | C/T | snv | 2 | |||
rs3205166 | 0.925 | 0.040 | 9 | 32459452 | synonymous variant | T/A;G | snv | 0.35 | 2 | ||
rs15895 | 1.000 | 0.040 | 12 | 113010483 | stop lost | A/G;T | snv | 0.75 | 1 | ||
rs371057322 | 0.925 | 0.040 | 2 | 8793960 | missense variant | T/C | snv | 1.4E-05 | 2 | ||
rs750898115 | 0.882 | 0.080 | 4 | 75787191 | missense variant | A/G | snv | 1.0E-05 | 3.5E-05 | 4 | |
rs763780 | 0.531 | 0.720 | 6 | 52236941 | missense variant | T/C | snv | 6.7E-02 | 6.6E-02 | 87 | |
rs3740360 | 0.827 | 0.240 | 10 | 94265734 | intron variant | A/C | snv | 9.7E-02 | 8.4E-02 | 7 | |
rs8177374 | 0.672 | 0.520 | 11 | 126292948 | missense variant | C/T | snv | 0.12 | 0.11 | 22 | |
rs12252 | 0.695 | 0.240 | 11 | 320772 | splice region variant | A/G | snv | 0.13 | 0.13 | 23 | |
rs6065 | 0.851 | 0.280 | 17 | 4933086 | missense variant | C/T | snv | 9.8E-02 | 0.13 | 6 | |
rs1805016 | 0.882 | 0.080 | 16 | 27363606 | missense variant | T/G | snv | 6.4E-02 | 0.13 | 3 | |
rs1800629 | 0.472 | 0.920 | 6 | 31575254 | upstream gene variant | G/A | snv | 0.12 | 0.14 | 169 | |
rs5745568 | 0.882 | 0.080 | 6 | 33580617 | intron variant | G/T | snv | 0.19 | 4 | ||
rs1799964 | 0.608 | 0.760 | 6 | 31574531 | upstream gene variant | T/C | snv | 0.19 | 47 | ||
rs1732778 | 0.882 | 0.080 | 12 | 113019120 | upstream gene variant | G/A | snv | 0.22 | 5 |