Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1883832 | 0.581 | 0.680 | 20 | 46118343 | 5 prime UTR variant | T/C | snv | 0.75 | 0.80 | 52 | |
rs4810485 | 0.732 | 0.480 | 20 | 46119308 | intron variant | T/A;G | snv | 16 | |||
rs1535045 | 0.742 | 0.360 | 20 | 46119460 | intron variant | C/A;G;T | snv | 12 | |||
rs772829518 | 0.925 | 0.200 | 20 | 46122699 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs4239702 | 1.000 | 0.120 | 20 | 46120612 | intron variant | T/C | snv | 0.75 | 1 |