Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4625 | 0.716 | 0.280 | 3 | 49534707 | 3 prime UTR variant | A/G | snv | 0.30 | 17 | ||
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 7 | ||
rs7225002 | 0.925 | 0.080 | 17 | 46111701 | intron variant | A/G | snv | 0.39 | 7 | ||
rs8067056 | 0.925 | 0.080 | 17 | 46006582 | intron variant | T/C;G | snv | 0.30 | 5 | ||
rs9303521 | 0.925 | 0.120 | 17 | 45727828 | intron variant | T/C;G | snv | 0.60 | 5 | ||
rs12938031 | 0.851 | 0.160 | 17 | 45777136 | intron variant | A/G | snv | 0.26 | 4 | ||
rs199505 | 0.925 | 0.120 | 17 | 46782044 | intron variant | A/G | snv | 0.84 | 4 | ||
rs62081501 | 0.925 | 0.080 | 18 | 37627749 | intron variant | G/A | snv | 6.2E-02 | 4 | ||
rs6774721 | 1.000 | 0.040 | 3 | 49344465 | upstream gene variant | G/A | snv | 0.15 | 4 | ||
rs7107356 | 1.000 | 0.040 | 11 | 47654618 | downstream gene variant | A/G | snv | 0.45 | 4 | ||
rs754593 | 1.000 | 0.040 | 17 | 45977330 | non coding transcript exon variant | G/A | snv | 0.52 | 4 | ||
rs8089865 | 1.000 | 0.040 | 18 | 53431552 | intron variant | G/A;C | snv | 4 | |||
rs10965780 | 1.000 | 0.040 | 9 | 23341717 | intron variant | C/G;T | snv | 3 | |||
rs111365677 | 0.925 | 0.040 | 1 | 99463578 | upstream gene variant | T/C | snv | 2.3E-03 | 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 | ||
rs113378111 | 1.000 | 0.040 | 2 | 9788024 | intergenic variant | G/A | snv | 2.8E-02 | 3 | ||
rs114465512 | 1.000 | 0.040 | 22 | 22047895 | intron variant | C/T | snv | 4.7E-03 | 3 | ||
rs117198528 | 1.000 | 0.040 | 18 | 49694188 | intergenic variant | T/G | snv | 1.0E-02 | 3 | ||
rs11924809 | 0.925 | 0.040 | 3 | 186353656 | intron variant | G/A | snv | 5.3E-02 | 3 | ||
rs12963463 | 1.000 | 0.040 | 18 | 55431862 | intron variant | C/G;T | snv | 3 | |||
rs138472420 | 1.000 | 0.040 | 19 | 47657765 | intron variant | G/A | snv | 3.3E-03 | 3 | ||
rs141746753 | 1.000 | 0.040 | 8 | 56934154 | intergenic variant | C/T | snv | 3.1E-03 | 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 |