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
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs1840680 0.807 0.200 3 157438240 intron variant A/G snv 0.59 6
rs368060
GBA
0.882 0.200 1 155235217 missense variant C/G snv 1.4E-04 7.7E-04 3