Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs746284240 0.763 0.240 12 68809243 missense variant A/G snv 11
rs934945 0.827 0.200 2 238246412 missense variant C/T snv 0.21 0.15 10
rs7602358 0.827 0.080 2 238147187 intron variant G/T snv 0.83 6
rs3027178 0.882 0.040 17 8149767 synonymous variant T/G snv 0.30 0.29 3