Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 | |
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
rs10930046 | 0.882 | 0.200 | 2 | 162281473 | missense variant | T/C | snv | 9.7E-02 | 0.16 | 3 | |
rs6432714 | 0.882 | 0.160 | 2 | 162280842 | intron variant | A/T | snv | 0.16 | 3 |