Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs568408 0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs747126003 0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06 18
rs12951053 0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs3213245 0.742 0.240 19 43575535 5 prime UTR variant G/A snv 0.65 0.60 13
rs7025417 0.752 0.280 9 6240084 intron variant T/C;G snv 11
rs12894467 0.807 0.080 14 101041390 non coding transcript exon variant C/T snv 0.51 0.50 6
rs171140 0.807 0.080 19 45361744 non coding transcript exon variant C/A snv 0.58 0.64 6
rs9895829 0.807 0.080 17 7675361 5 prime UTR variant A/G snv 7.4E-02 6