Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs138886989 | 0.925 | 0.160 | X | 101401763 | missense variant | T/C | snv | 1.9E-04 | 2.8E-05 | 2 | |
rs376685205 | 1.000 | 0.120 | 17 | 80105089 | missense variant | G/A;T | snv | 1.3E-04; 1.6E-05 | 1 | ||
rs397516354 | 0.790 | 0.120 | 19 | 55154094 | missense variant | C/A;G;T | snv | 4.0E-05 | 8 | ||
rs587782958 | 0.790 | 0.120 | 11 | 47333552 | splice region variant | C/T | snv | 1.7E-05 | 10 | ||
rs397516347 | 0.851 | 0.120 | 19 | 55154157 | missense variant | C/T | snv | 4.2E-05 | 5 | ||
rs121913638 | 0.851 | 0.120 | 14 | 23425980 | missense variant | C/T | snv | 4 | |||
rs1234386636 | 1.000 | 0.120 | 6 | 38723365 | missense variant | G/A | snv | 1 |