Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs61755783 | 0.763 | 0.080 | 6 | 42721911 | missense variant | G/A | snv | 1.4E-05 | 11 | ||
rs61755792 | 0.763 | 0.160 | 6 | 42721821 | missense variant | G/A;C | snv | 10 | |||
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 |