Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs10410544 0.827 0.120 19 38894892 intron variant T/C snv 0.68 0.67 6
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs7813 0.689 0.360 17 744946 missense variant G/A;C snv 0.63 22
rs7305115 0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56 8
rs2070951 0.776 0.320 4 148436862 splice region variant G/A;C snv 4.2E-06; 0.53 9
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2291739 0.925 0.080 12 56420869 missense variant G/A;C snv 0.49; 4.0E-06 6
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1044397 0.851 0.160 20 63349752 synonymous variant C/T snv 0.48 0.41 7
rs1044396 0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2077647 0.732 0.320 6 151807942 synonymous variant T/A;C snv 8.1E-06; 0.46 16
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs2522833 0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 7
rs13440581 0.882 0.080 X 151181399 missense variant A/G snv 0.45 0.45 5
rs561077 0.882 0.080 X 151181177 missense variant A/G snv 0.43 0.45 4
rs2291738 0.807 0.160 12 56421497 splice region variant T/C snv 0.43 0.39 8
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157