Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs80338671 | 0.851 | 0.120 | 3 | 81642787 | missense variant | T/C;G | snv | 4.5E-04; 3.2E-04 | 5 | ||
rs137852886 | 0.925 | 0.080 | 3 | 81648876 | missense variant | A/G | snv | 4.4E-06 | 2.1E-05 | 3 | |
rs201958741 | 0.851 | 0.120 | 3 | 81577999 | missense variant | C/T | snv | 3.3E-05 | 4.9E-05 | 3 | |
rs80338673 | 0.882 | 0.120 | 3 | 81577972 | missense variant | C/T | snv | 1.6E-05 | 3 | ||
rs869320698 | 1.000 | 3 | 81493813 | intron variant | CCACCACAC/ACCTGTCATGTAAAAAACA | delins | 1 |