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
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 18
rs7157599 0.925 0.040 14 100159565 missense variant C/T snv 0.73 0.76 6
rs75548401
GBA
0.882 0.160 1 155236246 missense variant G/A snv 5.9E-03 6.2E-03 6
rs761715536 1.000 0.040 10 111079092 stop gained G/A;T snv 6.4E-06; 1.3E-05 3