Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913315 | 0.882 | 0.160 | 19 | 1220488 | missense variant | G/A;T | snv | 5 | |||
rs121913323 | 1.000 | 0.040 | 19 | 1220416 | stop gained | C/T | snv | 2 | |||
rs137853080 | 1.000 | 0.040 | 19 | 1207058 | missense variant | T/G | snv | 2 | |||
rs137853081 | 1.000 | 0.040 | 19 | 1219352 | missense variant | G/C;T | snv | 2 |