Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs5780218 0.882 0.080 1 204196482 5 prime UTR variant A/- delins 0.44 4
rs13423759 0.925 0.080 2 211381247 3 prime UTR variant A/C snv 6.8E-02 3
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs11662595 0.882 0.120 18 24477006 missense variant A/G snv 8.6E-02 7.6E-02 7
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs13387042 0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 16
rs147574894 0.925 0.080 4 102600911 missense variant A/G snv 9.6E-05 3.9E-04 4
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs16940 0.882 0.080 17 43093220 synonymous variant A/G snv 0.35 0.29 5
rs172378 0.790 0.240 1 22638945 synonymous variant A/G snv 0.49 0.51 11
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2494752 0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs759478535 0.851 0.080 17 39708351 missense variant A/G snv 6.8E-05 4.2E-05 6
rs79036859 0.925 0.080 14 59369257 3 prime UTR variant A/G snv 3
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101