Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs743572 0.672 0.360 10 102837395 5 prime UTR variant A/G;T snv 0.40; 8.1E-06 24
rs10046 0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 18
rs2077647 0.732 0.320 6 151807942 synonymous variant T/A;C snv 8.1E-06; 0.46 16
rs2333227
MPO
0.752 0.320 17 58281401 upstream gene variant C/T snv 0.24 15
rs700519 0.752 0.280 15 51215771 missense variant G/A snv 7.6E-02 8.0E-02 11
rs7483 0.742 0.320 1 109737079 missense variant C/T snv 4.0E-06; 0.35 0.26 11