Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs148060787 | 0.851 | 0.080 | 11 | 61962853 | missense variant | C/G;T | snv | 4.4E-04 | 5 | ||
rs1800995 | 0.851 | 0.080 | 11 | 61955906 | missense variant | GC/AA | mnv | 5 | |||
rs1805142 | 0.851 | 0.080 | 11 | 61955825 | stop gained | G/C;T | snv | 2.7E-05 | 5 | ||
rs281865275 | 0.851 | 0.080 | 11 | 61957397 | missense variant | C/G;T | snv | 8.0E-06; 2.8E-05 | 5 | ||
rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 72 |