Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1064797078 | 1.000 | 0.080 | 3 | 48595159 | start lost | T/C | snv | 1 | |||
rs1064797079 | 1.000 | 0.080 | 3 | 48588988 | stop gained | -/TCAG | delins | 1 | |||
rs1064797080 | 1.000 | 0.080 | 3 | 48575678 | frameshift variant | TTCG/- | delins | 1 | |||
rs1064797081 | 1.000 | 0.080 | 3 | 48566686 | missense variant | C/T | snv | 1 | |||
rs1064797082 | 1.000 | 0.080 | 3 | 48581288 | frameshift variant | G/- | delins | 1 | |||
rs121912828 | 1.000 | 0.080 | 3 | 48566281 | missense variant | A/T | snv | 7.0E-06 | 1 | ||
rs121912830 | 1.000 | 0.080 | 3 | 48592613 | stop gained | G/A;T | snv | 7.2E-05 | 1 | ||
rs121912838 | 1.000 | 0.080 | 3 | 48575428 | missense variant | C/T | snv | 2.5E-05 | 2.1E-05 | 1 | |
rs121912849 | 1.000 | 0.080 | 3 | 48575236 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 1 | ||
rs121912851 | 1.000 | 0.080 | 3 | 48567736 | missense variant | C/T | snv | 1.4E-05 | 1 | ||
rs121912852 | 1.000 | 0.080 | 3 | 48570304 | stop gained | G/A | snv | 8.0E-06 | 1 | ||
rs121912853 | 1.000 | 0.080 | 3 | 48566719 | stop gained | C/A;T | snv | 1.2E-05 | 1 | ||
rs1333259313 | 1.000 | 0.080 | 3 | 48566545 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 1 | |
rs139318843 | 1.000 | 0.080 | 3 | 48568101 | missense variant | G/A | snv | 2.0E-05 | 4.9E-05 | 1 | |
rs1559423385 | 1.000 | 0.080 | 3 | 48587423 | stop gained | G/A | snv | 1 | |||
rs1559444716 | 1.000 | 0.080 | 3 | 48595076 | splice region variant | T/C | snv | 1 | |||
rs1560219171 | 1.000 | 0.080 | 3 | 48576286 | missense variant | C/T | snv | 1 | |||
rs730880286 | 1.000 | 0.080 | 3 | 48586378 | frameshift variant | G/- | delins | 1 | |||
rs755669902 | 1.000 | 0.080 | 3 | 48574549 | missense variant | C/T | snv | 1.2E-05 | 1.4E-05 | 1 | |
rs760891216 | 1.000 | 0.080 | 3 | 48568819 | missense variant | C/T | snv | 2.1E-05 | 7.0E-06 | 1 | |
rs766931219 | 1.000 | 0.080 | 3 | 48575445 | missense variant | C/G | snv | 4.2E-06 | 1 | ||
rs767182886 | 1.000 | 0.080 | 3 | 48578320 | splice donor variant | C/T | snv | 1 | |||
rs767539005 | 1.000 | 0.080 | 3 | 48574262 | splice region variant | C/T | snv | 5.6E-05 | 1 | ||
rs768128088 | 1.000 | 0.080 | 3 | 48573864 | frameshift variant | -/G | delins | 5.6E-05 | 1 | ||
rs775288140 | 1.000 | 0.080 | 3 | 48593101 | splice donor variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 1 |