Disease: Parkinson Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
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
rs356219
LOC105377329 ; SNCA
0.776 0.240 4 89716450 intron variant G/A snv 0.54 9
rs1800955
DRD4
0.827 0.160 11 636784 upstream gene variant T/C;G snv 8
rs156429
GPNMB
0.882 0.080 7 23266401 non coding transcript exon variant T/C snv 0.54 4
rs356200
SNCA
0.882 0.160 4 89747463 intron variant T/C snv 0.44 4
rs7033345
LINGO2
0.882 0.080 9 28717575 intergenic variant T/C;G snv 0.35 3