Source: BEFREE
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28904921 | 0.763 | 0.320 | 11 | 108329202 | missense variant | T/G | snv | 4.0E-05 | 6.3E-05 | 6 | |
rs769142993 | 0.851 | 0.280 | 11 | 108331498 | missense variant | G/C;T | snv | 2.4E-05 | 7.0E-06 | 5 | |
rs376676328 | 0.882 | 0.280 | 11 | 108353828 | missense variant | A/G | snv | 2.2E-04 | 1.8E-04 | 5 | |
rs587776551 | 1.000 | 0.200 | 11 | 108281168 | missense variant | G/A;T | snv | 1.6E-05 | 1.4E-05 | 3 | |
rs587781823 | 0.851 | 0.280 | 11 | 108284370 | frameshift variant | -/T | delins | 3 | |||
rs587779852 | 0.882 | 0.280 | 11 | 108312424 | stop gained | G/T | snv | 4.4E-05 | 3.5E-05 | 3 | |
rs730881333 | 0.882 | 0.280 | 11 | 108243994 | stop gained | C/A;T | snv | 4.1E-06; 8.1E-06 | 2 | ||
rs758081262 | 0.851 | 0.360 | 11 | 108267258 | stop gained | C/T | snv | 1.2E-05 | 2 | ||
rs768362387 | 0.851 | 0.360 | 11 | 108253846 | stop gained | C/A | snv | 2 | |||
rs587779872 | 1.000 | 0.200 | 11 | 108345818 | missense variant | C/T | snv | 3.2E-05 | 1.4E-05 | 2 | |
rs730881394 | 0.925 | 0.320 | 11 | 108310222 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 2 | |
rs564652222 | 0.925 | 0.280 | 11 | 108325416 | missense variant | C/A;T | snv | 1.4E-05 | 2 | ||
rs2234997 | 1.000 | 0.200 | 11 | 108235716 | missense variant | T/A | snv | 1.6E-02 | 6.1E-02 | 1 | |
rs587779815 | 1.000 | 0.200 | 11 | 108250804 | stop gained | C/T | snv | 8.0E-06 | 1.4E-05 | 1 | |
rs786202195 | 0.925 | 0.280 | 11 | 108251012 | stop gained | T/A;C;G | snv | 1 | |||
rs587782652 | 0.851 | 0.320 | 11 | 108335105 | missense variant | T/C | snv | 3.2E-05 | 4.2E-05 | 1 | |
rs770641163 | 0.882 | 0.360 | 11 | 108365208 | stop gained | C/G;T | snv | 4.0E-06; 1.2E-05 | 1 | ||
rs587782292 | 1.000 | 0.200 | 11 | 108365359 | missense variant | C/G;T | snv | 1.6E-05 | 2.1E-05 | 1 |