Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2477686 | 0.807 | 0.040 | 1 | 2461209 | intron variant | G/C | snv | 0.64 | 7 | ||
rs10842262 | 0.851 | 0.040 | 12 | 24031610 | intron variant | G/C | snv | 0.43 | 5 | ||
rs6080550 | 0.851 | 0.040 | 20 | 1778944 | intron variant | C/G;T | snv | 9.6E-02 | 5 | ||
rs12097821 | 0.882 | 0.040 | 1 | 106793679 | regulatory region variant | G/A;T | snv | 4 | |||
rs140506267 | 0.925 | 0.040 | 9 | 894044 | missense variant | A/G | snv | 2.7E-03 | 1.3E-03 | 2 |