Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7308720
LRRK2
0.790 0.120 12 40263898 missense variant C/A;G snv 4.0E-06; 8.7E-02 7
rs77369218
GBA
0.807 0.160 1 155235726 missense variant T/A snv 7
rs72824905
PLCG2
0.827 0.200 16 81908423 missense variant C/G;T snv 5.2E-03 6
rs104893936
SNCB
0.851 0.120 5 176626472 missense variant C/G;T snv 5.6E-05 4
rs104893937
SNCB
0.851 0.120 5 176621218 missense variant G/T snv 1.7E-04 2.0E-04 4
rs377591051
PRKN
0.851 0.080 6 162262651 missense variant C/T snv 4.0E-06 7.0E-06 4
rs113388242
EIF4G1
0.925 0.080 3 184327376 missense variant C/T snv 4.0E-05 7.0E-05 3
rs774457232
EIF4G1
0.925 0.080 3 184331303 missense variant G/A;T snv 6.4E-05 3
rs1041833271
APP
0.925 0.080 21 25975995 missense variant C/T snv 7.0E-06 2
rs1330229174
SNCA ; SNCA-AS1
0.925 0.080 4 89835568 missense variant T/C snv 4.0E-06 2
rs616338
ABI3
0.925 0.080 17 49219935 missense variant T/C snv 0.99 0.99 2
rs1342971994
SNCA
1.000 0.080 4 89822344 missense variant C/T snv 1.4E-05 1
rs897984
MIR762HG ; BCL7C ; MIR4519
0.925 0.080 16 30875322 non coding transcript exon variant T/C snv 0.62 0.47 2
rs1446915570
PSEN1
0.925 0.080 14 73173623 synonymous variant A/T snv 4.0E-06 7.0E-06 2
rs104886460
GBA
0.776 0.160 1 155240629 splice donor variant C/A;T snv 7.6E-05 8
rs777296100
SNCA
0.925 0.080 4 89725318 3 prime UTR variant -/TAA;TAAAA ins 2