Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1884444 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs3024490 0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs2280714 0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 10
rs2293152 0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05 10