Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs387906691 | 1.000 | 19 | 3595810 | missense variant | C/T | snv | 2 | ||||
rs1339688889 | 12 | 53315733 | missense variant | C/T | snv | 1 | |||||
rs1252993409 | 8 | 26864323 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |||
rs758865890 | 4 | 186288592 | missense variant | T/C | snv | 4.0E-06 | 1 | ||||
rs780463965 | 19 | 19626638 | missense variant | C/A;T | snv | 4.0E-06; 1.6E-05 | 1 | ||||
rs557043245 | 3 | 151338482 | missense variant | G/A | snv | 4.0E-05 | 7.0E-06 | 1 |