Disease: Parkinson Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs33939927
LRRK2
0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs34015634
LRRK2
0.851 0.120 12 40340380 missense variant T/C snv 3.2E-05 1.4E-05 8
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs34778348
LRRK2 ; LOC105369736
0.742 0.120 12 40363526 missense variant G/A snv 1.7E-03 5.8E-04 15
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
rs113994099
POLG
0.827 0.240 15 89320883 missense variant T/C snv 10
rs1290141855
SLC6A2
1.000 0.040 16 55698539 missense variant T/C snv 4.0E-06 7.0E-06 3
rs188286943
VPS35
0.776 0.160 16 46662452 missense variant C/T snv 9
rs5569
SLC6A2
0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs143624519
MAPT
0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs242557
MAPT
0.752 0.200 17 45942346 intron variant G/A snv 0.36 12
rs2942168
LINC02210-CRHR1 ; LINC02210
0.925 0.120 17 45637484 non coding transcript exon variant G/A;C;T snv 0.14 4
rs767543900
MAPT
0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs121918304
FBXO7
0.925 0.080 22 32498453 stop gained C/A;T snv 4.0E-06; 4.0E-06 4
rs1239756674
MAOA
1.000 0.040 X 43743818 synonymous variant G/A snv 2