Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9394309 | 0.851 | 0.040 | 6 | 35654004 | intron variant | G/A | snv | 0.74 | 4 | ||
rs9862857 | 0.851 | 0.040 | 3 | 30453840 | regulatory region variant | A/G;T | snv | 4 | |||
rs11082011 | 0.925 | 0.040 | 18 | 37565159 | intron variant | C/T | snv | 0.53 | 3 | ||
rs111365677 | 0.925 | 0.040 | 1 | 99463578 | upstream gene variant | T/C | snv | 2.3E-03 | 3 | ||
rs11155372 | 0.925 | 0.040 | 6 | 144698602 | intron variant | G/C;T | snv | 3 | |||
rs112106319 | 0.925 | 0.040 | 9 | 115094539 | intron variant | A/T | snv | 2.8E-03 | 3 | ||
rs112538845 | 0.925 | 0.040 | 4 | 184084475 | downstream gene variant | C/T | snv | 1.7E-02 | 3 | ||
rs11591827 | 0.925 | 0.040 | 10 | 81128126 | intergenic variant | G/A | snv | 8.4E-02 | 3 | ||
rs11728985 | 0.925 | 0.040 | 4 | 129115280 | 3 prime UTR variant | C/T | snv | 0.12 | 3 | ||
rs11924809 | 0.925 | 0.040 | 3 | 186353656 | intron variant | G/A | snv | 5.3E-02 | 3 | ||
rs11989919 | 0.882 | 0.040 | 8 | 32645107 | intron variant | T/C | snv | 0.10 | 3 | ||
rs11990063 | 0.925 | 0.040 | 8 | 10307685 | intron variant | C/A;T | snv | 3 | |||
rs12278912 | 0.882 | 0.040 | 11 | 124742263 | intron variant | G/A | snv | 0.33 | 3 | ||
rs12555870 | 0.925 | 0.040 | 9 | 23347726 | intron variant | A/G | snv | 0.36 | 3 | ||
rs139459337 | 0.882 | 0.040 | 3 | 114997018 | intron variant | C/T | snv | 4.7E-02 | 3 | ||
rs140504 | 0.882 | 0.040 | 22 | 23285182 | missense variant | A/G | snv | 0.81 | 0.86 | 3 | |
rs1411216 | 0.925 | 0.040 | 9 | 24520196 | intergenic variant | A/G | snv | 0.73 | 3 | ||
rs142484554 | 0.925 | 0.040 | 3 | 141059454 | intron variant | GAG/- | delins | 0.11 | 3 | ||
rs142641502 | 0.925 | 0.040 | 11 | 33109861 | intron variant | T/C | snv | 8.0E-03 | 3 | ||
rs1432441 | 0.882 | 0.040 | 15 | 66426943 | intron variant | G/A | snv | 0.27 | 3 | ||
rs143405544 | 0.925 | 0.040 | 5 | 65459777 | intron variant | A/G | snv | 4.8E-03 | 3 | ||
rs143934587 | 0.925 | 0.040 | 20 | 19165806 | intergenic variant | G/A | snv | 9.1E-03 | 3 | ||
rs1541187 | 0.882 | 0.040 | 1 | 147579693 | intron variant | C/G;T | snv | 3 | |||
rs1548076 | 0.925 | 0.040 | 15 | 69934284 | intergenic variant | G/A | snv | 0.95 | 3 | ||
rs1549854 | 0.882 | 0.040 | 15 | 66404397 | intron variant | A/C;G | snv | 0.44 | 3 |