Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10936599 | 0.637 | 0.600 | 3 | 169774313 | synonymous variant | C/T | snv | 0.29 | 0.21 | 15 | |
rs140522 | 0.851 | 0.160 | 22 | 50532837 | upstream gene variant | T/A;C | snv | 10 | |||
rs11755724 | 0.807 | 0.320 | 6 | 7118757 | intron variant | A/G;T | snv | 5 | |||
rs6793295 | 0.827 | 0.240 | 3 | 169800667 | missense variant | T/C;G | snv | 0.37; 1.8E-04 | 5 | ||
rs2777899 | 0.851 | 0.160 | 17 | 59755030 | intron variant | T/A;G | snv | 4 | |||
rs802734 | 0.827 | 0.280 | 6 | 127957653 | intergenic variant | A/G;T | snv | 4 | |||
rs806321 | 0.851 | 0.160 | 13 | 50267187 | intron variant | C/T | snv | 0.47 | 4 | ||
rs1292034 | 0.882 | 0.160 | 17 | 59912499 | intron variant | G/A | snv | 0.56 | 3 |