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
ALK
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
LPP
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
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64