Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11762634 | 7 | 141956687 | intron variant | G/A | snv | 0.22 | 1 | ||||
rs11767119 | 7 | 141912316 | intron variant | G/A | snv | 0.23 | 1 | ||||
rs11767947 | 7 | 141912821 | intron variant | G/A | snv | 0.23 | 1 | ||||
rs12539499 | 7 | 141930467 | intron variant | T/C | snv | 0.23 | 1 | ||||
rs17162635 | 7 | 141978163 | intron variant | T/A | snv | 1.0E-01 | 1 | ||||
rs4725559 | 7 | 141587852 | intron variant | G/A | snv | 0.36 | 1 | ||||
rs4726463 | 7 | 141666839 | intron variant | A/G | snv | 0.35 | 1 | ||||
rs4726481 | 7 | 141968603 | intron variant | G/T | snv | 0.43 | 1 | ||||
rs6976028 | 7 | 141912917 | intron variant | C/T | snv | 0.25 | 1 | ||||
rs713598 | 0.851 | 0.160 | 7 | 141973545 | missense variant | C/G | snv | 0.46 | 0.44 | 7 | |
rs10246939 | 0.851 | 0.240 | 7 | 141972804 | missense variant | T/C | snv | 0.49 | 0.47 | 6 | |
rs1726866 | 0.925 | 0.120 | 7 | 141972905 | missense variant | G/A | snv | 0.50 | 0.47 | 3 |