Source: INFERRED ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs61753219 | 0.672 | 0.400 | 6 | 42978330 | missense variant | G/A | snv | 3.6E-05 | 2.8E-05 | 64 | |
rs752298579 | 0.701 | 0.480 | 22 | 20061538 | missense variant | G/A | snv | 1.4E-04 | 7.0E-06 | 48 | |
rs1558939623 | 0.732 | 0.480 | 2 | 174824479 | missense variant | C/T | snv | 19 | |||
rs765379963 | 0.701 | 0.520 | 1 | 165743172 | stop gained | G/A | snv | 1.2E-05 | 2.1E-05 | 19 | |
rs771409809 | 0.732 | 0.480 | 4 | 6301794 | stop gained | C/T | snv | 6.0E-05 | 7.0E-06 | 19 | |
rs796053353 | 0.882 | 0.120 | 9 | 127661192 | missense variant | C/T | snv | 6 | |||
rs1567498374 | 0.882 | 0.160 | 16 | 75630493 | frameshift variant | G/-;GG | delins | 5 | |||
rs758723288 | 0.882 | 0.120 | 10 | 133370686 | missense variant | G/A | snv | 1.2E-05 | 1.4E-05 | 4 |