Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104893991 | 0.925 | 0.120 | 6 | 45438040 | missense variant | G/A | snv | 2 | |||
rs104893993 | 0.925 | 0.120 | 6 | 45437964 | missense variant | A/G | snv | 2 | |||
rs104893988 | 1.000 | 0.080 | 6 | 45512277 | stop gained | G/A | snv | 1 | |||
rs104893989 | 1.000 | 0.080 | 6 | 45431963 | missense variant | T/C;G | snv | 2.0E-05 | 1 | ||
rs104893990 | 1.000 | 0.080 | 6 | 45432011 | missense variant | G/A | snv | 1 | |||
rs104893992 | 1.000 | 0.080 | 6 | 45438039 | missense variant | C/T | snv | 1 | |||
rs104893994 | 1.000 | 0.080 | 6 | 45547304 | stop lost | G/C | snv | 1 | |||
rs104893995 | 1.000 | 0.080 | 6 | 45431945 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
rs1057521068 | 1.000 | 0.080 | 6 | 45432008 | missense variant | G/A | snv | 1 | |||
rs1428979499 | 1.000 | 0.080 | 6 | 45431875 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs201647225 | 1.000 | 0.080 | 6 | 45431962 | missense variant | A/G | snv | 1.1E-04 | 6.3E-05 | 1 | |
rs397515537 | 1.000 | 0.080 | 6 | 45546910 | stop gained | C/T | snv | 1 | |||
rs397515538 | 1.000 | 0.080 | 6 | 45422618 | frameshift variant | C/-;CC | delins | 1 | |||
rs730880313 | 1.000 | 0.080 | 6 | 45422723 | frameshift variant | GCAGCAACAGCAGCA/ACAGCAGCAGCAGCAGCAGCAACAGCAGCCG | delins | 1 | |||
rs730880315 | 1.000 | 0.080 | 6 | 45546964 | frameshift variant | -/C | delins | 1 | |||
rs752933596 | 1.000 | 0.080 | 6 | 45438020 | missense variant | A/T | snv | 1 | |||
rs759100705 | 1.000 | 0.080 | 6 | 45431872 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
rs864621970 | 1.000 | 0.080 | 6 | 45431915 | missense variant | G/A | snv | 1 |