Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12203592 | 0.649 | 0.320 | 6 | 396321 | intron variant | C/T | snv | 0.10 | 38 | ||
rs1805007 | 0.695 | 0.280 | 16 | 89919709 | missense variant | C/A;G;T | snv | 4.4E-02 | 25 | ||
rs1805008 | 0.732 | 0.240 | 16 | 89919736 | missense variant | C/T | snv | 4.7E-02 | 4.8E-02 | 16 | |
rs885479 | 0.732 | 0.280 | 16 | 89919746 | missense variant | G/A | snv | 0.15 | 8.3E-02 | 16 | |
rs12913832 | 0.763 | 0.200 | 15 | 28120472 | intron variant | A/G | snv | 0.50 | 15 | ||
rs16891982 | 0.776 | 0.200 | 5 | 33951588 | missense variant | C/A;G | snv | 0.65 | 13 | ||
rs864745 | 0.763 | 0.320 | 7 | 28140937 | intron variant | T/C | snv | 0.41 | 12 | ||
rs1800407 | 0.807 | 0.200 | 15 | 27985172 | missense variant | C/T | snv | 4.7E-02 | 4.9E-02 | 10 | |
rs6059655 | 0.790 | 0.080 | 20 | 34077942 | intron variant | A/G | snv | 0.95 | 10 | ||
rs17833789 | 0.807 | 0.080 | 17 | 57153267 | intergenic variant | C/A | snv | 0.37 | 8 | ||
rs1129038 | 0.851 | 0.120 | 15 | 28111713 | 3 prime UTR variant | C/T | snv | 0.49 | 0.50 | 8 | |
rs1805005 | 0.827 | 0.080 | 16 | 89919436 | missense variant | G/T | snv | 8.6E-02 | 8.0E-02 | 8 | |
rs1805006 | 0.790 | 0.080 | 16 | 89919510 | missense variant | C/A;G | snv | 5.2E-03; 4.0E-06 | 8 | ||
rs9392504 | 0.827 | 0.120 | 6 | 412802 | downstream gene variant | G/A | snv | 0.44 | 7 | ||
rs1393350 | 0.851 | 0.160 | 11 | 89277878 | intron variant | G/A | snv | 0.17 | 7 | ||
rs1042602 | 0.925 | 0.080 | 11 | 89178528 | missense variant | C/A | snv | 0.25 | 0.24 | 6 | |
rs6782181 | 0.851 | 0.160 | 3 | 138386212 | intron variant | G/A;C | snv | 6 | |||
rs4778138 | 0.851 | 0.080 | 15 | 28090674 | intron variant | A/G;T | snv | 6 | |||
rs4911414 | 0.882 | 0.120 | 20 | 34141638 | regulatory region variant | T/G | snv | 0.73 | 5 | ||
rs1667394 | 15 | 28285036 | intron variant | C/A;T | snv | 5 | |||||
rs916977 | 1.000 | 0.080 | 15 | 28268218 | intron variant | T/C;G | snv | 5 | |||
rs121918166 | 0.925 | 0.160 | 15 | 27985101 | missense variant | C/T | snv | 3.0E-03 | 3.4E-03 | 5 | |
rs74653330 | 0.851 | 0.200 | 15 | 27983407 | missense variant | C/T | snv | 8.4E-03 | 6.2E-03 | 5 | |
rs6707137 | 0.882 | 0.040 | 2 | 88254832 | regulatory region variant | G/A | snv | 0.12 | 4 | ||
rs12931267 | 1.000 | 0.040 | 16 | 89752324 | intron variant | C/G | snv | 4.7E-02 | 4 |