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
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs1475170339
IGFALS ; SPSB3
0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs34778348
LRRK2 ; LOC105369736
0.742 0.120 12 40363526 missense variant G/A snv 1.7E-03 5.8E-04 15
rs62643364
PRNP
0.851 0.160 20 4699466 synonymous variant A/G;T snv 4.0E-06; 1.4E-04 7
rs11931074
SNCA ; LOC105377329
0.851 0.080 4 89718364 intron variant G/A;C;T snv 7
rs1224426272
CIT
0.925 0.040 12 119869138 missense variant C/T snv 6
rs387907264
PFN1
0.851 0.080 17 4946742 missense variant A/C snv 5
rs2435207
MAPT
1.000 0.040 17 45981562 intron variant G/A snv 0.30 2
rs6821591
PPARGC1A
1.000 0.040 4 23795377 3 prime UTR variant C/T snv 0.53 2
rs7665116
PPARGC1A
4 23851388 intron variant T/A;C snv 1