Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2710102 | 0.790 | 0.120 | 7 | 147877298 | intron variant | A/G;T | snv | 1 | |||
rs352759 | 0.925 | 0.040 | 8 | 15742205 | intron variant | T/A | snv | 3 | |||
rs9364726 | 0.882 | 0.040 | 6 | 164236705 | intergenic variant | A/G | snv | 6.5E-02 | 3 | ||
rs112538845 | 0.925 | 0.040 | 4 | 184084475 | downstream gene variant | C/T | snv | 1.7E-02 | 3 | ||
rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 1 | |||
rs11924809 | 0.925 | 0.040 | 3 | 186353656 | intron variant | G/A | snv | 5.3E-02 | 3 | ||
rs11829119 | 0.851 | 0.040 | 12 | 19040597 | intergenic variant | T/A;C | snv | 4 | |||
rs143934587 | 0.925 | 0.040 | 20 | 19165806 | intergenic variant | G/A | snv | 9.1E-03 | 3 | ||
rs10405744 | 0.851 | 0.040 | 19 | 19948684 | intron variant | G/A | snv | 9.0E-02 | 4 | ||
rs6740584 | 0.882 | 0.040 | 2 | 207564627 | intron variant | T/C | snv | 0.37 | 1 | ||
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 7 | ||
rs78087832 | 0.925 | 0.040 | 2 | 224600060 | intergenic variant | C/T | snv | 2.4E-03 | 3 | ||
rs12555870 | 0.925 | 0.040 | 9 | 23347726 | intron variant | A/G | snv | 0.36 | 3 | ||
rs6586354 | 0.851 | 0.040 | 1 | 234897489 | intron variant | G/A | snv | 0.25 | 4 | ||
rs2302045 | 0.851 | 0.040 | 2 | 241081801 | splice region variant | G/A | snv | 7.6E-02 | 1.0E-01 | 4 | |
rs1411216 | 0.925 | 0.040 | 9 | 24520196 | intergenic variant | A/G | snv | 0.73 | 3 | ||
rs200855945 | 0.925 | 0.040 | 12 | 26124961 | 5 prime UTR variant | ACACGCACAC/-;ACACGCACACACACGCACAC | delins | 1.6E-02 | 3 | ||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 8 | |
rs1401635 | 0.925 | 0.040 | 11 | 27672444 | intron variant | C/G | snv | 0.73 | 2 | ||
rs183124483 | 0.925 | 0.040 | 17 | 28110028 | intron variant | G/A | snv | 7.1E-04 | 3 | ||
rs853679 | 0.851 | 0.160 | 6 | 28329086 | intron variant | C/A | snv | 0.20 | 4 | ||
rs10968749 | 0.851 | 0.040 | 9 | 28752486 | intergenic variant | A/G | snv | 5.5E-02 | 4 | ||
rs9862857 | 0.851 | 0.040 | 3 | 30453840 | regulatory region variant | A/G;T | snv | 4 | |||
rs4512342 | 0.827 | 0.120 | 8 | 32750356 | intron variant | T/G | snv | 0.12 | 1 | ||
rs17673138 | 0.851 | 0.040 | 8 | 32840440 | intron variant | A/C | snv | 8.6E-02 | 4 |