Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs56149945 | 0.595 | 0.680 | 5 | 143399752 | missense variant | T/A;C | snv | 2.0E-02 | 49 | ||
rs74315329 | 0.732 | 0.240 | 1 | 171636338 | stop gained | G/A | snv | 1.1E-03 | 8.7E-04 | 15 | |
rs74315328 | 0.807 | 0.120 | 1 | 171636131 | missense variant | A/G | snv | 6 | |||
rs566289099 | 0.807 | 0.080 | 1 | 171636310 | missense variant | G/A | snv | 2.0E-05 | 3.5E-05 | 6 | |
rs7859156 | 0.851 | 0.040 | 9 | 126637749 | intron variant | T/C | snv | 0.74 | 4 | ||
rs2761884 | 0.925 | 0.120 | 14 | 53954334 | intron variant | G/T | snv | 0.34 | 3 | ||
rs7854658 | 0.882 | 0.040 | 9 | 126652659 | intron variant | G/A | snv | 0.26 | 3 | ||
rs4986888 | 0.925 | 0.040 | 2 | 38071026 | missense variant | G/A;C | snv | 4.4E-03 | 2 |