Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs104894718 0.790 0.160 19 35033654 stop gained C/A;G;T snv 4.0E-06 8
rs3812718 0.776 0.240 2 166053034 splice region variant C/T snv 0.48 8
rs16990018 0.882 0.120 20 4699732 missense variant A/G snv 3.8E-03 1.6E-02 5