Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113388242
EIF4G1
0.925 0.080 3 184327376 missense variant C/T snv 4.0E-05 7.0E-05 3
rs104893936
SNCB
0.851 0.120 5 176626472 missense variant C/G;T snv 5.6E-05 4
rs774457232
EIF4G1
0.925 0.080 3 184331303 missense variant G/A;T snv 6.4E-05 3
rs104886460
GBA
0.776 0.160 1 155240629 splice donor variant C/A;T snv 7.6E-05 8
rs1064651
GBA
0.732 0.360 1 155235727 missense variant C/G snv 1.3E-04 2.0E-04 13
rs104893937
SNCB
0.851 0.120 5 176621218 missense variant G/T snv 1.7E-04 2.0E-04 4
rs75822236
GBA
0.752 0.200 1 155235002 missense variant C/T snv 1.8E-04 6.1E-05 10
rs112176450
EIF4G1
0.807 0.080 3 184327401 missense variant G/A;T snv 2.1E-04 2.8E-04 7
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs72824905
PLCG2
0.827 0.200 16 81908423 missense variant C/G;T snv 5.2E-03 6
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs897984
MIR762HG ; BCL7C ; MIR4519
0.925 0.080 16 30875322 non coding transcript exon variant T/C snv 0.62 0.47 2
rs616338
ABI3
0.925 0.080 17 49219935 missense variant T/C snv 0.99 0.99 2