Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs112295309 1.000 0.080 8 143813896 missense variant T/C;G snv 6.1E-04 3
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs121913369 0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 12
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480