Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs199473058 | 0.925 | 0.080 | 3 | 38630341 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs199473101 | 0.925 | 0.080 | 3 | 38606682 | missense variant | C/A;T | snv | 8.1E-06 | 2 | ||
rs199473169 | 0.925 | 0.080 | 3 | 38585821 | missense variant | T/G | snv | 2 | |||
rs199473172 | 0.925 | 0.080 | 3 | 38585800 | missense variant | C/A;T | snv | 4.0E-06 | 2 | ||
rs199473292 | 0.925 | 0.080 | 3 | 38551391 | missense variant | C/G;T | snv | 2 | |||
rs199473305 | 0.925 | 0.080 | 3 | 38551145 | missense variant | C/T | snv | 1.4E-05 | 2 | ||
rs199473554 | 0.925 | 0.080 | 3 | 38630392 | missense variant | C/T | snv | 2 | |||
rs28937318 | 0.925 | 0.080 | 3 | 38606709 | missense variant | C/A;T | snv | 2 | |||
rs727505158 | 0.925 | 0.080 | 3 | 38599005 | frameshift variant | G/- | delins | 1.4E-05 | 2 | ||
rs794728843 | 0.925 | 0.080 | 3 | 38620842 | splice donor variant | C/T | snv | 7.0E-06 | 2 | ||
rs886037904 | 0.925 | 0.080 | 3 | 38554272 | coding sequence variant | -/CCAC | delins | 2 | |||
rs137854600 | 0.807 | 0.120 | 3 | 38551504 | missense variant | C/A;T | snv | 4 | |||
rs137854601 | 0.776 | 0.120 | 3 | 38551022 | stop gained | C/A;T | snv | 4.0E-06 | 6 | ||
rs137854604 | 0.882 | 0.120 | 3 | 38551243 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 3 | |
rs137854611 | 0.882 | 0.120 | 3 | 38597787 | missense variant | G/A;C;T | snv | 4.0E-06 | 3 | ||
rs137854612 | 0.851 | 0.120 | 3 | 38560170 | missense variant | C/T | snv | 4 | |||
rs137854618 | 0.742 | 0.120 | 3 | 38566426 | missense variant | C/A;T | snv | 8.0E-06 | 8 | ||
rs199473062 | 0.827 | 0.120 | 3 | 38622401 | stop gained | C/A;G;T | snv | 4.1E-06 | 3 | ||
rs199473097 | 0.763 | 0.120 | 3 | 38606710 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 9 | |
rs199473153 | 0.882 | 0.120 | 3 | 38597737 | stop gained | C/A;T | snv | 4.0E-06 | 3 | ||
rs199473220 | 0.882 | 0.120 | 3 | 38562422 | missense variant | C/A | snv | 4.2E-05 | 2.8E-05 | 3 | |
rs199473225 | 0.851 | 0.120 | 3 | 38560397 | missense variant | G/A;C | snv | 3 | |||
rs199473266 | 0.882 | 0.120 | 3 | 38555697 | missense variant | G/C | snv | 2.0E-05 | 3 | ||
rs199473282 | 0.827 | 0.120 | 3 | 38551513 | missense variant | G/A;T | snv | 4.0E-06 | 4 | ||
rs199473556 | 0.851 | 0.120 | 3 | 38630342 | missense variant | G/A | snv | 2 |