Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4647924 | 0.600 | 0.520 | 4 | 1801844 | missense variant | C/A;G;T | snv | 4.2E-06; 4.2E-06 | 49 | ||
rs1555745467 | 0.752 | 0.240 | 19 | 13262771 | missense variant | C/A | snv | 23 | |||
rs758946412 | 0.790 | 0.240 | X | 100407507 | frameshift variant | G/-;GG | delins | 12 | |||
rs121909673 | 0.776 | 0.080 | 5 | 162093965 | missense variant | G/A | snv | 10 | |||
rs774843232 | 0.851 | 0.080 | 11 | 3825024 | missense variant | G/A;C;T | snv | 8.0E-06; 3.6E-05; 1.2E-05 | 9 | ||
rs1557644984 | 0.925 | 0.080 | 1 | 42927622 | missense variant | A/G | snv | 5 | |||
rs41292285 | 1.000 | 0.040 | 16 | 1208033 | missense variant | G/T | snv | 7.3E-03 | 7.1E-03 | 3 | |
rs540638287 | 1.000 | 0.040 | 16 | 1204313 | missense variant | C/T | snv | 4.3E-05 | 1.4E-05 | 3 |