Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs61747728 | 0.701 | 0.240 | 1 | 179557079 | missense variant | C/T | snv | 3.0E-02 | 2.8E-02 | 20 | |
rs138545216 | 1.000 | 0.120 | 1 | 179557094 | missense variant | C/T | snv | 4.0E-05 | 1.0E-04 | 1 | |
rs188942711 | 0.763 | 0.200 | 2 | 227253336 | missense variant | G/A;T | snv | 2.8E-05; 4.0E-06 | 9 | ||
rs35138315 | 0.882 | 0.200 | 2 | 227052367 | stop gained | G/C | snv | 6.8E-05 | 1.1E-04 | 3 | |
rs375290088 | 0.925 | 0.120 | 2 | 227303904 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 2 | |
rs1269093075 | 1.000 | 0.120 | 2 | 227253324 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
rs1308023279 | 1.000 | 0.120 | 2 | 227280483 | missense variant | G/C | snv | 1.4E-05 | 1 | ||
rs35423326 | 1.000 | 0.120 | 19 | 35861122 | missense variant | G/A | snv | 2.9E-02 | 3.0E-02 | 1 | |
rs104886142 | 0.790 | 0.280 | X | 108598793 | missense variant | G/A | snv | 8.7E-05 | 4.7E-05 | 10 |