Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs4833095 0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28