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
rs10680577 0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 16
rs314276 0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs3756712 0.790 0.160 5 308981 non coding transcript exon variant A/C;T snv 10
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
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
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
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
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs33917957
MET
0.790 0.120 7 116700208 missense variant A/G snv 2.7E-02 1.8E-02 10
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs4645878
BAX
0.882 0.120 19 48954681 upstream gene variant A/G snv 0.89 5