Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs281860566 | 1.000 | 0.080 | 6 | 31270339 | missense variant | C/T | snv | 1 | |||
rs760454379 | 1.000 | 0.080 | 7 | 50400082 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 1 | |
rs12573787 | 1.000 | 0.080 | 10 | 87863959 | 5 prime UTR variant | G/A;C | snv | 1 | |||
rs1257378 | 1.000 | 0.080 | 11 | 94621792 | intron variant | A/T | snv | 1 | |||
rs9610915 | 1.000 | 0.080 | 22 | 38215073 | 3 prime UTR variant | C/G | snv | 0.48 | 0.41 | 1 | |
rs754736070 | 1.000 | 0.080 | 4 | 99597206 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 1 | |
rs1414109649 | 1.000 | 0.080 | 5 | 40765164 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
rs369488601 | 1.000 | 0.080 | 22 | 23181175 | missense variant | G/A;C | snv | 1.9E-05; 9.7E-05 | 1 | ||
rs775014154 | 1.000 | 0.080 | 22 | 23181637 | missense variant | C/T | snv | 5.8E-05 | 7.0E-05 | 1 | |
rs1178702025 | 1.000 | 0.080 | 18 | 44951912 | missense variant | G/A | snv | 1 | |||
rs1057519771 | 1.000 | 0.080 | 9 | 130872201 | missense variant | G/C | snv | 2 | |||
rs121913454 | 0.925 | 0.080 | 9 | 130874969 | missense variant | A/G | snv | 2 | |||
rs121913460 | 0.925 | 0.080 | 9 | 130862971 | missense variant | A/T | snv | 2 | |||
rs1314838108 | 0.925 | 0.160 | 9 | 130854977 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
rs111340708 | 0.925 | 0.080 | 12 | 111447548 | intron variant | TGGGGTGGGGTGGGG/-;TGGGG;TGGGGTGGGG;TGGGGTGGGGTGGGGTGGGG;TGGGGTGGGGTGGGGTGGGGTGGGG | delins | 0.52 | 2 | ||
rs918140013 | 0.925 | 0.080 | 12 | 111447663 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
rs121913505 | 0.925 | 0.080 | 4 | 54695598 | missense variant | G/A | snv | 2.0E-05 | 2 | ||
rs137852974 | 0.925 | 0.200 | 11 | 62691132 | stop gained | G/A | snv | 4.0E-06 | 2 | ||
rs1208076129 | 0.925 | 0.120 | 6 | 31164861 | stop gained | G/A | snv | 4.1E-06 | 2.1E-05 | 2 | |
rs1483790387 | 0.925 | 0.120 | 5 | 115625762 | missense variant | C/A | snv | 2 | |||
rs141157255 | 0.882 | 0.120 | 12 | 98659331 | missense variant | G/A | snv | 4.0E-05 | 2.8E-05 | 3 | |
rs3092856 | 0.882 | 0.120 | 11 | 108289005 | missense variant | C/T | snv | 1.2E-02 | 2.2E-02 | 3 | |
rs1407906280 | 0.882 | 0.120 | 12 | 68839467 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs4148356 | 0.851 | 0.120 | 16 | 16083418 | missense variant | G/A | snv | 2.3E-02 | 1.3E-02 | 4 | |
rs45511401 | 0.851 | 0.120 | 16 | 16079375 | missense variant | G/T | snv | 3.8E-02 | 3.6E-02 | 4 |