Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs221798 | 0.882 | 0.040 | 7 | 100689872 | intron variant | C/A;G | snv | 3 | |||
rs221774 | 0.851 | 0.080 | 7 | 100701361 | upstream gene variant | A/G;T | snv | 4 | |||
rs506597 | 0.882 | 0.040 | 7 | 100715797 | upstream gene variant | A/G | snv | 0.90 | 4 | ||
rs11191454 | 0.776 | 0.160 | 10 | 102900247 | intron variant | A/G | snv | 7.9E-02 | 5 | ||
rs7914558 | 0.851 | 0.040 | 10 | 103016151 | intron variant | G/A | snv | 0.40 | 5 | ||
rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 12 | ||
rs9297357 | 0.851 | 0.040 | 8 | 105130105 | intron variant | C/G;T | snv | 5 | |||
rs6738485 | 0.882 | 0.040 | 2 | 106193504 | intron variant | C/T | snv | 0.36 | 3 | ||
rs12871532 | 0.851 | 0.040 | 13 | 108016199 | intergenic variant | T/C | snv | 0.46 | 5 | ||
rs56031956 | 0.882 | 0.040 | 9 | 108863349 | missense variant | C/G | snv | 2.3E-02 | 2.2E-02 | 3 | |
rs7959663 | 0.925 | 0.040 | 12 | 109446562 | intron variant | G/A;C | snv | 2 | |||
rs77867520 | 0.882 | 0.040 | 4 | 11186225 | intergenic variant | C/T | snv | 7.2E-02 | 3 | ||
rs17158930 | 0.851 | 0.040 | 7 | 111871082 | intron variant | A/G | snv | 0.25 | 4 | ||
rs9577511 | 0.882 | 0.040 | 13 | 113337508 | intron variant | A/G | snv | 0.15 | 4 | ||
rs7939917 | 0.882 | 0.040 | 11 | 113697374 | missense variant | C/T | snv | 2.0E-03 | 9.2E-03 | 3 | |
rs26318 | 0.925 | 0.040 | 5 | 116352208 | intron variant | C/T | snv | 0.99 | 3 | ||
rs61945387 | 0.882 | 0.040 | 12 | 117921609 | intron variant | A/G | snv | 7.7E-02 | 3 | ||
rs61123830 | 0.925 | 0.040 | 11 | 123522138 | intron variant | G/A | snv | 0.37 | 2 | ||
rs4870888 | 0.882 | 0.040 | 8 | 124096736 | intron variant | T/C | snv | 0.39 | 4 | ||
rs548181 | 0.851 | 0.040 | 11 | 125591814 | 5 prime UTR variant | A/G | snv | 0.83 | 5 | ||
rs201048567 | 0.882 | 0.040 | 7 | 125615031 | intergenic variant | CA/- | delins | 1.0E-05 | 3 | ||
rs137928907 | 0.882 | 0.040 | 12 | 130827204 | missense variant | A/C | snv | 1.4E-02 | 1.5E-02 | 3 | |
rs7405404 | 0.925 | 0.040 | 16 | 13656002 | intergenic variant | T/A;C | snv | 3 | |||
rs105633 | 0.882 | 0.040 | 5 | 141945684 | synonymous variant | T/C;G | snv | 0.98; 4.0E-06 | 3 | ||
rs141252918 | 0.882 | 0.040 | 6 | 151506923 | intron variant | G/A;C | snv | 4 |