Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs7133914
LRRK2
0.790 0.120 12 40309109 missense variant G/A;T snv 8.5E-02; 1.6E-05 7
rs72824905
PLCG2
0.827 0.200 16 81908423 missense variant C/G;T snv 5.2E-03 6
rs7308720
LRRK2
0.790 0.120 12 40263898 missense variant C/A;G snv 4.0E-06; 8.7E-02 7
rs75822236
GBA
0.752 0.200 1 155235002 missense variant C/T snv 1.8E-04 6.1E-05 10
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs7681440
SNCA-AS1 ; SNCA
1.000 0.080 4 89835399 intron variant C/A;G snv 1
rs77369218
GBA
0.807 0.160 1 155235726 missense variant T/A snv 7
rs774457232
EIF4G1
0.925 0.080 3 184331303 missense variant G/A;T snv 6.4E-05 3
rs777296100
SNCA
0.925 0.080 4 89725318 3 prime UTR variant -/TAA;TAAAA ins 2
rs78973108
GBA
0.776 0.160 1 155237453 missense variant C/T snv 2.8E-05 4.2E-05 8
rs80356769
GBA
0.776 0.160 1 155235772 missense variant C/A snv 3.2E-05 7.0E-06 8
rs80356771
GBA
0.776 0.160 1 155235196 missense variant G/A;T snv 7.2E-05; 4.0E-06 8
rs897984
MIR762HG ; BCL7C ; MIR4519
0.925 0.080 16 30875322 non coding transcript exon variant T/C snv 0.62 0.47 2