Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750306 0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs28936379 0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs1108580
DBH
0.790 0.240 9 133639992 splice region variant A/G snv 0.45 0.54 9
rs2344484 0.925 0.040 5 135540941 upstream gene variant A/G snv 0.47 3
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs33939927 0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs80356537 0.752 0.320 19 41970405 missense variant C/A;G;T snv 17
rs121909668
FUS
0.790 0.120 16 31191418 missense variant C/A;G;T snv 1.2E-05 8
rs371425292
APP
0.763 0.160 21 25897627 missense variant C/A;T snv 8.0E-06 10
rs387906709 0.776 0.120 X 56565363 missense variant C/A;T snv 9
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs104893878 0.732 0.160 4 89835580 missense variant C/G snv 21
rs1315695444 1.000 0.040 1 169611580 missense variant C/G snv 4.0E-06 1.4E-05 2
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
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
rs63750424 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 18
rs1223904774
APP
0.790 0.120 21 25891772 missense variant C/T snv 4.0E-06 7.0E-06 8
rs7157599 0.925 0.040 14 100159565 missense variant C/T snv 0.73 0.76 6
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78