Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs17879469 0.763 0.360 6 32584333 missense variant C/G snv 1.3E-05 9
rs3792876 0.790 0.280 5 132301616 intron variant C/T snv 6.9E-02 7
rs2291282 0.882 0.120 17 42346547 intron variant T/C snv 1.2E-03 3.4E-04 3