Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs11210892 1.000 0.040 1 43634413 intergenic variant G/A snv 0.51 3
rs4664442 1.000 0.040 2 161971491 intron variant G/A;C snv 3
rs11783093 1.000 0.040 8 27567832 intron variant C/T snv 0.11 2