Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs61816761 | 0.658 | 0.640 | 1 | 152313385 | stop gained | G/A;T | snv | 9.4E-03; 8.0E-06 | 43 | ||
rs33980500 | 0.742 | 0.200 | 6 | 111592059 | missense variant | C/T | snv | 8.6E-02 | 9.7E-02 | 14 | |
rs281875214 | 0.790 | 0.160 | 17 | 80183976 | missense variant | A/C | snv | 7 | |||
rs1347671835 | 0.827 | 0.160 | 16 | 88639888 | missense variant | C/A;G | snv | 4.3E-06 | 5 | ||
rs179363865 | 0.882 | 0.080 | X | 154563613 | missense variant | G/C | snv | 3 | |||
rs9267502 | 1.000 | 0.040 | 6 | 31585417 | upstream gene variant | G/A | snv | 7.6E-02 | 1 |