Disease: Parkinson Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11701
RNASE4 ; ANG
0.925 0.080 14 20693894 synonymous variant T/A;C;G snv 4.0E-06; 0.14 2
rs1572931
RAB29 ; LOC105371702
0.925 0.080 1 205775090 splice region variant C/A;T snv 0.14 2
rs591486
ERCC6L2
0.925 0.080 9 95887764 intron variant A/G snv 0.44 2
rs148156462
COQ2
0.925 0.080 4 83264287 missense variant A/G snv 4.2E-03 1.6E-03 3
rs2275294
ZNF512B
0.925 0.080 20 63962894 intron variant G/A snv 0.25 3
rs34016896
LOC105374187
0.925 0.080 3 161275076 regulatory region variant C/T snv 0.28 3
rs356220
LOC105377329 ; SNCA
0.925 0.080 4 89720189 intron variant T/A;C snv 3
rs2736990
SNCA
0.882 0.080 4 89757390 intron variant G/A;T snv 4
rs267606929
OPTN
0.827 0.120 10 13132098 missense variant A/G snv 5
rs7224296
LRRC37A2 ; NSF
0.882 0.160 17 46722680 intron variant G/A snv 0.59 5
rs80356718
TARDBP
0.827 0.120 1 11022209 missense variant A/G snv 7.6E-05 4.9E-05 5
rs142444896
CHCHD2
0.807 0.120 7 56106409 missense variant G/A snv 9.3E-03 7.5E-03 6
rs17571
CTSD
0.827 0.120 11 1761364 missense variant G/A snv 7.0E-02 6.2E-02 6
rs3794087
SLC1A2
0.851 0.120 11 35308068 intron variant G/T snv 0.20 6
rs35801418
LRRK2
0.827 0.120 12 40321114 missense variant A/G snv 7
rs3849942
C9orf72 ; LOC107987057
0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 9
rs121909334
VCP
0.752 0.200 9 35065255 missense variant C/T snv 1.6E-05 10
rs121909329
VCP
0.763 0.200 9 35065363 missense variant C/A;G;T snv 11
rs121909330
VCP
0.752 0.200 9 35065364 missense variant G/A;C;T snv 11
rs11868035
RAI1 ; SREBF1
0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 14
rs121912443
SOD1
0.732 0.160 21 31663857 missense variant A/G snv 15
rs367543041
TARDBP
0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs11558538
LOC107985948 ; HNMT
0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 19
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28