Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs118101777 | 0.614 | 0.280 | 15 | 90087472 | missense variant | C/T | snv | 2.0E-03 | 1.6E-03 | 42 | |
rs121913503 | 0.689 | 0.200 | 15 | 90088606 | missense variant | C/A;T | snv | 23 | |||
rs121913502 | 0.708 | 0.320 | 15 | 90088702 | missense variant | C/A;T | snv | 3.2E-05 | 19 | ||
rs1057519736 | 0.752 | 0.160 | 15 | 90088605 | missense variant | C/G | snv | 13 | |||
rs267606870 | 0.763 | 0.280 | 15 | 90088703 | missense variant | G/A;C | snv | 11 | |||
rs1057519906 | 0.882 | 0.120 | 15 | 90088607 | missense variant | T/A;C | snv | 8 | |||
rs1042026735 | 1.000 | 0.040 | 15 | 90088650 | synonymous variant | G/A | snv | 1 | |||
rs200758694 | 1.000 | 0.040 | 15 | 90088686 | synonymous variant | C/A;G;T | snv | 6.8E-05; 4.0E-06; 6.0E-05 | 1 | ||
rs773159667 | 1.000 | 0.040 | 15 | 90087549 | synonymous variant | G/A | snv | 8.0E-06 | 1 |