Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 214 | |||
rs878854066 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 213 | |||
rs28934576 | 0.554 | 0.600 | 17 | 7673802 | missense variant | C/A;G;T | snv | 4.0E-06; 1.6E-05 | 78 | ||
rs1057520005 | 0.742 | 0.360 | 17 | 7673800 | missense variant | C/A;G | snv | 14 | |||
rs1060501201 | 0.925 | 0.080 | 17 | 7674190 | missense variant | T/C;G | snv | 4 | |||
rs267605077 | 0.925 | 0.080 | 17 | 7675212 | missense variant | A/G;T | snv | 3 | |||
rs138983188 | 0.925 | 0.080 | 17 | 7674863 | missense variant | G/A;T | snv | 4.0E-06 | 2 | ||
rs143458271 | 0.925 | 0.080 | 17 | 7676589 | synonymous variant | C/T | snv | 9.2E-05 | 8.4E-05 | 2 |