Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs797046134 | 1.000 | 0.040 | 15 | 100914748 | missense variant | T/C | snv | 1 | |||
rs1553920379 | 0.776 | 0.160 | 4 | 101032294 | frameshift variant | -/AGTA | delins | 27 | |||
rs1566823361 | 0.742 | 0.440 | 13 | 101726732 | frameshift variant | -/G | delins | 18 | |||
rs34002892 | 0.851 | 0.200 | 12 | 101753470 | frameshift variant | GA/- | delins | 5.1E-04 | 3.5E-04 | 8 | |
rs1409313 | 1.000 | 0.040 | 10 | 102431844 | intron variant | T/C | snv | 0.85 | 1 | ||
rs11191454 | 0.776 | 0.160 | 10 | 102900247 | intron variant | A/G | snv | 7.9E-02 | 5 | ||
rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 12 | ||
rs7910584 | 1.000 | 0.040 | 10 | 106607970 | intron variant | C/A | snv | 0.65 | 1 | ||
rs11211996 | 1.000 | 0.040 | 11 | 106987949 | intron variant | T/C | snv | 0.15 | 1 | ||
rs1895729 | 1.000 | 0.040 | 11 | 107113002 | intergenic variant | G/A | snv | 0.37 | 1 | ||
rs10749886 | 1.000 | 0.040 | 11 | 107129809 | intergenic variant | G/A | snv | 0.35 | 1 | ||
rs3797817 | 1.000 | 0.040 | 5 | 108948641 | intron variant | A/C;G | snv | 1 | |||
rs4773054 | 1.000 | 0.040 | 13 | 109501681 | intron variant | T/C | snv | 0.89 | 2 | ||
rs10498676 | 0.925 | 0.040 | 6 | 11026766 | intron variant | G/A | snv | 0.18 | 1 | ||
rs12877501 | 0.925 | 0.160 | 13 | 110512039 | missense variant | G/A;C | snv | 5.0E-04 | 4 | ||
rs6891903 | 1.000 | 0.040 | 5 | 11371193 | intron variant | A/G | snv | 6.8E-02 | 1 | ||
rs3782000 | 1.000 | 0.040 | 11 | 114202153 | intron variant | C/T | snv | 0.18 | 1 | ||
rs6537825 | 1.000 | 0.040 | 1 | 114405659 | missense variant | A/G | snv | 0.88 | 0.92 | 1 | |
rs11582563 | 1.000 | 0.040 | 1 | 114416918 | intron variant | G/A | snv | 0.14 | 1 | ||
rs11585926 | 1.000 | 0.040 | 1 | 114431068 | intron variant | T/C | snv | 0.22 | 3 | ||
rs11589568 | 1.000 | 0.040 | 1 | 114453702 | intron variant | T/C | snv | 0.14 | 1 | ||
rs7511633 | 1.000 | 0.040 | 1 | 114456655 | intron variant | G/A | snv | 0.36 | 1 | ||
rs6661053 | 1.000 | 0.040 | 1 | 114496497 | intron variant | T/A;C | snv | 1 | |||
rs11102800 | 1.000 | 0.040 | 1 | 114498310 | intron variant | C/T | snv | 0.58 | 2 | ||
rs3827735 | 1.000 | 0.040 | 1 | 114510087 | intron variant | C/A;T | snv | 1 |