Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9332964 | 0.763 | 0.240 | 2 | 31529325 | missense variant | C/T | snv | 4.7E-04 | 1.6E-04 | 10 | |
rs121913494 | 0.827 | 0.240 | 20 | 58909541 | missense variant | A/G;T | snv | 7 | |||
rs9332969 | 0.827 | 0.240 | X | 67722899 | missense variant | G/A;T | snv | 5 | |||
rs1386577803 | 0.851 | 0.240 | X | 67722872 | missense variant | G/A | snv | 4 | |||
rs763296857 | 0.882 | 0.200 | 2 | 31529427 | missense variant | T/C | snv | 1.6E-05 | 2.8E-05 | 3 |