Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv 10
rs6269
COMT ; MIR4761
0.827 0.240 22 19962429 5 prime UTR variant A/G snv 0.38 10
rs660895
HLA-DRB1
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 10
rs1169089134
FOLH1
0.790 0.320 11 49206785 missense variant C/G;T snv 9
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs188286943
VPS35
0.776 0.160 16 46662452 missense variant C/T snv 9
rs356219
LOC105377329 ; SNCA
0.776 0.240 4 89716450 intron variant G/A snv 0.54 9
rs35870237
LRRK2
0.763 0.120 12 40340404 missense variant T/C snv 9
rs3849942
C9orf72 ; LOC107987057
0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 9
rs431905511
SNCA
0.827 0.080 4 89828154 missense variant C/T snv 9
rs6438552
GSK3B
0.790 0.280 3 119912967 intron variant A/G snv 0.54 9
rs738499
TEF ; LOC105373042
0.851 0.120 22 41381096 intron variant G/T snv 0.76 9
rs1800955
DRD4
0.827 0.160 11 636784 upstream gene variant T/C;G snv 8
rs35652124
NFE2L2
0.790 0.320 2 177265345 intron variant T/C snv 0.29 8
rs4784227
CASC16
0.807 0.160 16 52565276 intron variant C/T snv 0.20 8
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv 8
rs760077
MTX1 ; THBS3
0.925 0.120 1 155208991 missense variant T/A snv 0.36 8
rs104894104
CDKN2A
0.790 0.160 9 21971019 missense variant G/A;T snv 7
rs11931074
SNCA ; LOC105377329
0.851 0.080 4 89718364 intron variant G/A;C;T snv 7
rs2287161
MTERF2
0.827 0.080 12 106987362 upstream gene variant C/G;T snv 7
rs2295633
FAAH
0.827 0.120 1 46408711 intron variant A/G;T snv 7
rs28363170
SLC6A3
0.827 0.120 5 1393745 3 prime UTR variant -/AGTGGGGGCCCTGCATGCGTCCTGGGGTAGTACACGCTCC delins 8.1E-06 7
rs28938172
PARK7
0.790 0.080 1 7984981 missense variant T/C snv 7
rs34995376
LRRK2
0.807 0.080 12 40310435 missense variant G/A snv 7.0E-06 7
rs35801418
LRRK2
0.827 0.120 12 40321114 missense variant A/G snv 7