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
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs144848 0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs1799977 0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs5918 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 26
rs156697 0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 24
rs2227982 0.677 0.480 2 241851281 missense variant G/A snv 9.2E-02 4.3E-02 24
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs17561 0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23
rs238406 0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs1899663 0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs34301344 0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22
rs2066827 0.695 0.320 12 12718165 missense variant T/A;C;G snv 1.6E-04; 1.6E-05; 0.26 21