Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs75932628 | 0.662 | 0.480 | 6 | 41161514 | missense variant | C/A;T | snv | 6.8E-05; 2.6E-03 | 28 | ||
rs104894002 | 0.790 | 0.320 | 6 | 41161557 | stop gained | G/A | snv | 2.0E-05 | 2.1E-05 | 7 | |
rs2234253 | 0.827 | 0.120 | 6 | 41161367 | missense variant | G/A;C;T | snv | 1.9E-04; 1.0E-02 | 5 | ||
rs753325601 | 0.851 | 0.200 | 6 | 41161515 | missense variant | G/A | snv | 2.8E-05 | 7.0E-06 | 4 | |
rs121908402 | 0.882 | 0.280 | 6 | 41161277 | missense variant | A/C | snv | 1.2E-05 | 3 | ||
rs2234256 | 0.882 | 0.120 | 6 | 41158917 | missense variant | A/G | snv | 1.8E-02 | 4.0E-02 | 3 | |
rs766647311 | 0.882 | 0.080 | 6 | 41159841 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 3 | ||
rs142232675 | 1.000 | 0.080 | 6 | 41161395 | missense variant | C/T | snv | 9.7E-04 | 1.5E-03 | 1 | |
rs143332484 | 1.000 | 0.080 | 6 | 41161469 | missense variant | C/A;T | snv | 7.6E-03 | 1 | ||
rs201280312 | 1.000 | 0.080 | 6 | 41161265 | missense variant | G/A | snv | 8.0E-06 | 1 | ||
rs150277350 | 1.000 | 0.080 | 6 | 41158975 | missense variant | C/T | snv | 1.4E-04 | 9.8E-05 | 1 | |
rs149622783 | 1.000 | 0.080 | 6 | 41159867 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-04 | 1 | ||
rs2234255 | 1.000 | 0.080 | 6 | 41159805 | missense variant | G/A | snv | 4.9E-03 | 1.8E-03 | 1 |