Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs3218373 0.827 0.120 7 152677078 upstream gene variant C/A snv 0.15 5