Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121912532 | 0.776 | 0.280 | 2 | 48688065 | missense variant | C/A;G;T | snv | 1.2E-05 | 12 | ||
rs121912535 | 0.827 | 0.240 | 2 | 48688427 | missense variant | A/C | snv | 6 | |||
rs121912518 | 0.882 | 0.160 | 2 | 48688064 | missense variant | T/C;G | snv | 5 | |||
rs121912526 | 0.882 | 0.040 | 2 | 48688604 | missense variant | A/G | snv | 4 | |||
rs121912534 | 0.882 | 0.040 | 2 | 48688094 | missense variant | G/A;T | snv | 3 | |||
rs121912540 | 0.882 | 0.040 | 2 | 48688106 | missense variant | T/C | snv | 3 | |||
rs1046910653 | 0.925 | 0.040 | 11 | 35206151 | missense variant | C/T | snv | 2 | |||
rs121912522 | 0.925 | 0.040 | 2 | 48688082 | missense variant | G/A;C | snv | 2 | |||
rs774592723 | 0.925 | 0.040 | 11 | 35204551 | missense variant | C/T | snv | 4.0E-06 | 2 |