Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113994095 | 0.701 | 0.360 | 15 | 89327201 | missense variant | C/T | snv | 5.1E-04 | 6.7E-04 | 31 | |
rs113994097 | 0.724 | 0.400 | 15 | 89323426 | missense variant | C/G | snv | 9.7E-04 | 7.9E-04 | 22 | |
rs267606959 | 0.732 | 0.200 | 15 | 89318986 | missense variant | G/A | snv | 2.0E-05 | 19 | ||
rs143319805 | 0.807 | 0.320 | 3 | 193643378 | missense variant | A/G | snv | 6.2E-04 | 5.7E-04 | 12 | |
rs113994099 | 0.827 | 0.240 | 15 | 89320883 | missense variant | T/C | snv | 10 | |||
rs201477273 | 0.851 | 0.120 | 15 | 89320857 | missense variant | G/A | snv | 6.8E-04 | 3.4E-04 | 5 | |
rs1177373525 | 0.925 | 0.080 | 3 | 193666331 | missense variant | A/G | snv | 1.2E-05 | 2 |