Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113871094 | 0.683 | 0.320 | 15 | 48465820 | stop gained | G/A | snv | 34 | |||
rs727503057 | 0.708 | 0.280 | 15 | 48505106 | missense variant | G/A | snv | 7.0E-06 | 16 | ||
rs727503054 | 0.732 | 0.200 | 15 | 48420752 | missense variant | A/G;T | snv | 1.6E-05 | 15 | ||
rs1555397413 | 0.732 | 0.280 | 15 | 48470705 | missense variant | T/C | snv | 13 | |||
rs137854480 | 0.742 | 0.200 | 15 | 48537629 | missense variant | G/A | snv | 11 | |||
rs730880099 | 0.742 | 0.200 | 15 | 48510125 | missense variant | G/A | snv | 11 | |||
rs193922185 | 0.752 | 0.200 | 15 | 48505037 | missense variant | G/A | snv | 10 | |||
rs397515757 | 0.752 | 0.200 | 15 | 48515382 | splice region variant | C/T | snv | 10 | |||
rs794728195 | 0.752 | 0.200 | 15 | 48495155 | missense variant | G/A | snv | 10 | |||
rs111401431 | 0.763 | 0.200 | 15 | 48468097 | missense variant | G/A | snv | 9 | |||
rs111984349 | 0.763 | 0.200 | 15 | 48415759 | missense variant | C/T | snv | 9 | |||
rs113543334 | 0.763 | 0.200 | 15 | 48432944 | missense variant | A/G | snv | 9 | |||
rs140583 | 0.763 | 0.200 | 15 | 48495219 | stop gained | G/A | snv | 9 | |||
rs1555400373 | 0.763 | 0.200 | 15 | 48515393 | missense variant | A/G | snv | 9 | |||
rs193922204 | 0.763 | 0.200 | 15 | 48468542 | splice region variant | C/T | snv | 4.0E-06 | 7.0E-06 | 9 | |
rs193922228 | 0.763 | 0.200 | 15 | 48430736 | missense variant | A/G | snv | 7.0E-06 | 9 | ||
rs794728334 | 0.763 | 0.200 | 15 | 48437069 | stop gained | C/A;T | snv | 9 | |||
rs1555397718 | 0.776 | 0.200 | 15 | 48474566 | missense variant | C/A;T | snv | 8 | |||
rs1566899590 | 0.776 | 0.200 | 15 | 48448894 | splice acceptor variant | C/T | snv | 8 | |||
rs1566911957 | 0.776 | 0.200 | 15 | 48496204 | frameshift variant | GTACACATTCA/- | delins | 8 | |||
rs71467648 | 0.776 | 0.200 | 15 | 48437898 | stop gained | A/C;T | snv | 8 | |||
rs794728208 | 0.776 | 0.200 | 15 | 48485374 | missense variant | C/T | snv | 8 |