Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs112735431 | 0.683 | 0.320 | 17 | 80385145 | missense variant | G/A;C | snv | 2.6E-04; 8.0E-06 | 24 | ||
rs5029939 | 0.701 | 0.440 | 6 | 137874586 | intron variant | C/G | snv | 0.13 | 19 | ||
rs137852741 | 0.807 | 0.120 | 2 | 202556360 | stop gained | C/G;T | snv | 4.0E-06 | 7 | ||
rs1085307252 | 0.882 | 0.080 | 2 | 202518890 | missense variant | A/T | snv | 3 | |||
rs1085307253 | 0.882 | 0.080 | 2 | 202518890 | frameshift variant | AG/T | delins | 3 | |||
rs137852749 | 0.882 | 0.080 | 2 | 202552774 | missense variant | G/A | snv | 3 |