Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10019009 0.851 0.080 4 87661983 missense variant A/G;T snv 4.0E-06; 0.29 4
rs1005464 0.882 0.040 20 6775501 intron variant G/A snv 0.19 5
rs10208273 0.882 0.040 2 6383862 intergenic variant A/G snv 0.30 3
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1052667 0.882 0.040 19 47004177 3 prime UTR variant C/G;T snv 6
rs1056629 0.827 0.120 16 82148499 3 prime UTR variant T/C snv 0.14 6
rs1057519736 0.752 0.160 15 90088605 missense variant C/G snv 13
rs1057519902 0.742 0.160 1 226064451 missense variant G/C snv 16
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1060501205 0.827 0.120 17 7673749 missense variant TG/GT mnv 5
rs1061970 0.882 0.040 17 50184491 3 prime UTR variant A/G snv 0.13 3
rs11177386 0.882 0.040 12 68820362 missense variant G/A snv 3
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1131691003 0.752 0.360 17 7676381 splice donor variant C/A;G snv 12
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1131691042 0.752 0.360 17 7675052 splice donor variant C/T snv 12
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs11866002 0.851 0.120 16 58553833 synonymous variant C/T snv 0.35 0.39 4
rs12146774 1.000 0.040 12 119235698 intron variant C/T snv 0.15 1
rs1215600806 0.851 0.120 1 21564100 missense variant T/C snv 1.2E-05 4