Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104893956 | 1.000 | 6 | 151842613 | stop gained | C/T | snv | 1 | ||||
rs1131692059 | 1.000 | 6 | 152011740 | missense variant | G/A | snv | 1 | ||||
rs1562787582 | 1.000 | 6 | 152099207 | 3 prime UTR variant | T/A | snv | 1 | ||||
rs397509428 | 1.000 | 6 | 152011684 | missense variant | G/T | snv | 1 | ||||
rs776119905 | 1.000 | 1 | 54032127 | 3 prime UTR variant | C/A;G;T | snv | 4.1E-06; 4.1E-06 | 1 | |||
rs6929137 | 0.851 | 0.160 | 6 | 151615542 | missense variant | G/A | snv | 0.31 | 0.36 | 6 | |
rs2046210 | 0.708 | 0.280 | 6 | 151627231 | intergenic variant | G/A | snv | 0.41 | 21 |