Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs78311289 | 0.689 | 0.440 | 4 | 1806162 | missense variant | A/C;G | snv | 4.0E-06 | 4 | ||
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 1 | ||
rs1057519713 | 0.925 | 0.120 | 4 | 54736498 | missense variant | G/C | snv | 1 | |||
rs121913514 | 0.763 | 0.240 | 4 | 54733174 | missense variant | T/A;G | snv | 1 | |||
rs757545210 | 1.000 | 0.120 | 5 | 172105697 | missense variant | T/C | snv | 1 | |||
rs137853078 | 0.925 | 0.120 | 19 | 1220396 | missense variant | G/A | snv | 1 |