Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519893 | 0.790 | 0.160 | 12 | 56085070 | missense variant | G/A;T | snv | 8 | |||
rs1057519891 | 0.851 | 0.160 | 12 | 56088557 | missense variant | G/A;T | snv | 4.0E-06 | 5 | ||
rs1057519892 | 0.851 | 0.160 | 12 | 56088558 | missense variant | A/T | snv | 5 | |||
rs1057519803 | 0.925 | 0.080 | 12 | 56088138 | missense variant | G/A | snv | 2 | |||
rs931676601 | 12 | 56097196 | missense variant | A/G;T | snv | 1 | |||||
rs1057519817 | 12 | 56088073 | missense variant | C/A;G | snv | 4.0E-06 | 1 | ||||
rs755855285 | 12 | 56102035 | missense variant | G/A | snv | 1.1E-04 | 1.4E-04 | 1 |