Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs16991720 | 21 | 34484464 | intron variant | A/C | snv | 4 | |||||
rs1801689 | 17 | 66214462 | missense variant | A/C;G | snv | 4.0E-06; 2.4E-02; 4.8E-05 | 7 | ||||
rs2980875 | 8 | 125469505 | intron variant | A/C;G;T | snv | 6 | |||||
rs10789117 | 1 | 62606594 | intron variant | A/C;T | snv | 5 | |||||
rs10518982 | 15 | 58507555 | intron variant | A/G | snv | 2.2E-02 | 3 | ||||
rs11668477 | 0.925 | 0.080 | 19 | 11084354 | downstream gene variant | A/G | snv | 0.34 | 7 | ||
rs11925396 | 3 | 194391622 | downstream gene variant | A/G | snv | 1.9E-02 | 3 | ||||
rs1535 | 0.752 | 0.240 | 11 | 61830500 | intron variant | A/G | snv | 0.31 | 24 | ||
rs1713222 | 2 | 21048451 | upstream gene variant | A/G | snv | 0.82 | 3 | ||||
rs17321515 | 0.776 | 0.200 | 8 | 125474167 | intron variant | A/G | snv | 0.49 | 16 | ||
rs1874148 | 10 | 74114657 | intron variant | A/G | snv | 1.8E-02 | 6 | ||||
rs2001844 | 0.882 | 0.040 | 8 | 125466503 | upstream gene variant | A/G | snv | 0.43 | 9 | ||
rs2075650 | 0.662 | 0.360 | 19 | 44892362 | intron variant | A/G | snv | 0.13 | 0.13 | 45 | |
rs2303790 | 0.724 | 0.280 | 16 | 56983380 | missense variant | A/G | snv | 2.6E-03 | 6.5E-04 | 19 | |
rs2678379 | 1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 | 8 | ||
rs28917504 | 12 | 6814956 | missense variant | A/G | snv | 1.5E-03 | 6.4E-03 | 4 | |||
rs2954021 | 1.000 | 0.040 | 8 | 125469835 | intron variant | A/G | snv | 0.54 | 15 | ||
rs33980385 | 19 | 40991388 | missense variant | A/G | snv | 6 | |||||
rs370911 | 1 | 162323515 | intron variant | A/G | snv | 0.99 | 6 | ||||
rs4251583 | 12 | 43783705 | missense variant | A/G | snv | 8.6E-04 | 1.1E-03 | 6 | |||
rs4385188 | 5 | 75438537 | intron variant | A/G | snv | 0.33 | 4 | ||||
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 43 | ||
rs4803750 | 0.807 | 0.240 | 19 | 44744370 | upstream gene variant | A/G | snv | 7.7E-02 | 22 | ||
rs5020 | 17 | 44255219 | splice region variant | A/G | snv | 3.2E-03 | 1.3E-02 | 3 | |||
rs562338 | 0.807 | 0.160 | 2 | 21065449 | intergenic variant | A/G | snv | 0.69 | 21 |