Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs5029939 0.701 0.440 6 137874586 intron variant C/G snv 0.13 19