Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34811474 1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs3791679 0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs143384 0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 13
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24