Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1136410 | 0.559 | 0.760 | 1 | 226367601 | missense variant | A/G | snv | 0.21 | 0.15 | 70 | |
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs4072037 | 0.732 | 0.240 | 1 | 155192276 | splice acceptor variant | C/A;T | snv | 0.59 | 22 | ||
rs5275 | 0.583 | 0.560 | 1 | 186673926 | 3 prime UTR variant | A/G;T | snv | 55 | |||
rs533748068 | 0.851 | 0.080 | 1 | 155950962 | missense variant | C/A;T | snv | 4.3E-06 | 7.0E-06 | 5 | |
rs595961 | 0.807 | 0.160 | 1 | 35902179 | intron variant | A/G | snv | 0.30 | 0.37 | 6 | |
rs1056836 | 0.581 | 0.680 | 2 | 38071060 | missense variant | G/C | snv | 0.51 | 58 | ||
rs1057519784 | 0.827 | 0.080 | 2 | 29220765 | missense variant | G/T | snv | 7 | |||
rs4953354 | 0.827 | 0.120 | 2 | 46348249 | intron variant | A/G | snv | 0.22 | 5 | ||
rs772399455 | 0.851 | 0.080 | 2 | 15942096 | missense variant | G/A;C | snv | 4.0E-06 | 6 | ||
rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 71 | ||
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
rs1064607 | 0.827 | 0.200 | 3 | 188877884 | 3 prime UTR variant | G/C | snv | 0.46 | 5 | ||
rs10937405 | 0.807 | 0.080 | 3 | 189665394 | intron variant | C/T | snv | 0.38 | 9 | ||
rs121913279 | 0.526 | 0.560 | 3 | 179234297 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 101 | ||
rs2073498 | 0.763 | 0.280 | 3 | 50332115 | missense variant | C/A | snv | 9.6E-02 | 8.0E-02 | 12 | |
rs2131877 | 0.827 | 0.080 | 3 | 195137645 | intron variant | G/A | snv | 0.20 | 6 | ||
rs425366 | 0.851 | 0.080 | 3 | 283727 | intron variant | A/C | snv | 0.56 | 4 | ||
rs4488809 | 0.827 | 0.080 | 3 | 189638472 | intron variant | T/C | snv | 0.45 | 5 | ||
rs63750447 | 0.716 | 0.200 | 3 | 37025749 | missense variant | T/A | snv | 2.7E-03 | 7.5E-04 | 17 | |
rs6790167 | 0.827 | 0.080 | 3 | 189869485 | intron variant | A/G | snv | 0.53 | 5 | ||
rs775439790 | 0.851 | 0.080 | 3 | 9765858 | missense variant | T/C | snv | 8.0E-06 | 1.4E-05 | 4 | |
rs876658657 | 0.677 | 0.280 | 3 | 37020356 | missense variant | A/G | snv | 4.0E-06 | 25 | ||
rs7041 | 0.576 | 0.800 | 4 | 71752617 | missense variant | A/C;T | snv | 0.52; 4.0E-06 | 64 |