Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs201921722 | 0.925 | 0.040 | 11 | 123679999 | downstream gene variant | -/A | delins | 9.2E-06 | 3 | ||
rs188843168 | 0.925 | 0.040 | 10 | 103390184 | intron variant | T/A;C | snv | 4.3E-04 | 3 | ||
rs182377406 | 0.925 | 0.040 | 11 | 67449378 | upstream gene variant | A/G | snv | 4.5E-04 | 3 | ||
rs183124483 | 0.925 | 0.040 | 17 | 28110028 | intron variant | G/A | snv | 7.1E-04 | 3 | ||
rs189864513 | 0.925 | 0.040 | 4 | 52767390 | intron variant | T/C | snv | 1.9E-03 | 3 | ||
rs111365677 | 0.925 | 0.040 | 1 | 99463578 | upstream gene variant | T/C | snv | 2.3E-03 | 3 | ||
rs78087832 | 0.925 | 0.040 | 2 | 224600060 | intergenic variant | C/T | snv | 2.4E-03 | 3 | ||
rs112106319 | 0.925 | 0.040 | 9 | 115094539 | intron variant | A/T | snv | 2.8E-03 | 3 | ||
rs80278479 | 0.925 | 0.040 | 6 | 50758466 | intron variant | C/G | snv | 3.0E-03 | 3 | ||
rs143405544 | 0.925 | 0.040 | 5 | 65459777 | intron variant | A/G | snv | 4.8E-03 | 3 | ||
rs77945277 | 0.925 | 0.040 | 14 | 34840969 | intron variant | A/G | snv | 4.9E-03 | 3 | ||
rs142641502 | 0.925 | 0.040 | 11 | 33109861 | intron variant | T/C | snv | 8.0E-03 | 3 | ||
rs143934587 | 0.925 | 0.040 | 20 | 19165806 | intergenic variant | G/A | snv | 9.1E-03 | 3 | ||
rs190783615 | 0.925 | 0.040 | X | 142772620 | intergenic variant | T/C | snv | 9.3E-03 | 3 | ||
rs201569130 | 0.925 | 0.040 | 6 | 1402916 | intergenic variant | GACA/- | delins | 1.1E-02 | 3 | ||
rs200855945 | 0.925 | 0.040 | 12 | 26124961 | 5 prime UTR variant | ACACGCACAC/-;ACACGCACACACACGCACAC | delins | 1.6E-02 | 3 | ||
rs112538845 | 0.925 | 0.040 | 4 | 184084475 | downstream gene variant | C/T | snv | 1.7E-02 | 3 | ||
rs16935279 | 0.851 | 0.040 | 8 | 68961217 | intron variant | T/C | snv | 1.9E-02 | 4 | ||
rs75921243 | 0.925 | 0.040 | 8 | 9988356 | intron variant | T/G | snv | 1.9E-02 | 2 | ||
rs56388524 | 0.925 | 0.040 | 5 | 45757459 | intergenic variant | C/A;T | snv | 2.0E-02 | 3 | ||
rs77826363 | 0.882 | 0.040 | 6 | 1128802 | intergenic variant | G/T | snv | 2.2E-02 | 3 | ||
rs183042538 | 0.925 | 0.040 | 20 | 41197420 | intron variant | A/T | snv | 3.2E-02 | 3 | ||
rs17156280 | 0.925 | 0.040 | 7 | 82414674 | intron variant | T/C | snv | 3.4E-02 | 2 | ||
rs2017122 | 0.925 | 0.040 | 11 | 118444134 | intron variant | C/T | snv | 4.0E-02 | 2 | ||
rs73425402 | 0.925 | 0.040 | 12 | 77503518 | intron variant | T/A | snv | 4.1E-02 | 3 |