Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12052498 | 2 | 189497185 | intergenic variant | G/A | snv | 0.39 | 2 | ||||
rs144403535 | 2 | 62178025 | regulatory region variant | A/G | snv | 3.8E-03 | 2 | ||||
rs2698530 | 2 | 64276761 | intergenic variant | A/C | snv | 0.23 | 2 | ||||
rs61784830 | 1 | 45763401 | intergenic variant | G/A | snv | 8.9E-02 | 2 | ||||
rs78455250 | 1 | 189052039 | intergenic variant | G/A;C | snv | 2 | |||||
rs183360145 | 6 | 25296893 | intron variant | T/C | snv | 2.6E-03 | 2 | ||||
rs56071727 | 1 | 45625172 | upstream gene variant | G/T | snv | 9.0E-02 | 2 | ||||
rs187281066 | 3 | 132157410 | intron variant | A/G | snv | 1.4E-05 | 2 | ||||
rs112409831 | 3 | 132417596 | 5 prime UTR variant | C/T | snv | 2.3E-02 | 2 | ||||
rs183252871 | 3 | 134964503 | intron variant | T/C;G | snv | 2 | |||||
rs187472012 | 3 | 134820915 | intron variant | A/G | snv | 2.7E-04 | 2 | ||||
rs78545713 | 6 | 26248612 | upstream gene variant | A/G;T | snv | 2 | |||||
rs9813476 | 3 | 197992314 | intron variant | C/T | snv | 3.7E-02 | 2 | ||||
rs74138220 | 1 | 189188129 | intergenic variant | G/A | snv | 3.8E-03 | 2 | ||||
rs145285408 | 7 | 11345523 | intron variant | G/C | snv | 2.4E-03 | 2 | ||||
rs142692454 | 1 | 36686538 | intergenic variant | A/G | snv | 4.1E-03 | 2 | ||||
rs16839481 | 3 | 132660153 | 5 prime UTR variant | G/A | snv | 1.1E-02 | 2 | ||||
rs61740410 | 6 | 27256809 | downstream gene variant | G/A | snv | 4.2E-02 | 2 | ||||
rs7637997 | 3 | 133864120 | intron variant | G/A;C;T | snv | 2 | |||||
rs9824310 | 3 | 159474954 | intron variant | A/G | snv | 0.68 | 2 | ||||
rs9872999 | 3 | 133738670 | intron variant | C/G;T | snv | 2 | |||||
rs183511413 | 3 | 133330418 | intron variant | A/G | snv | 2.3E-04 | 2 | ||||
rs192622883 | 3 | 133150563 | intron variant | A/G | snv | 2.5E-04 | 2 | ||||
rs80215559 | 6 | 25917997 | intron variant | T/C | snv | 3.7E-02 | 3 | ||||
rs8177248 | 1.000 | 0.040 | 3 | 133760782 | non coding transcript exon variant | C/T | snv | 0.28 | 3 |