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
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs33939927 0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs104893875 0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs2306604 0.827 0.080 10 58388932 intron variant A/C;G;T snv 5