Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs121912443
SOD1
0.732 0.160 21 31663857 missense variant A/G snv 15
rs104894201
CRYAB
0.763 0.280 11 111908934 missense variant T/C snv 12
rs104893768
RHO
0.807 0.080 3 129528801 missense variant C/A snv 11
rs121909329
VCP
0.763 0.200 9 35065363 missense variant C/A;G;T snv 11
rs431905511
SNCA
0.827 0.080 4 89828154 missense variant C/T snv 9
rs63750311
PSEN1
0.790 0.240 14 73192647 missense variant A/C snv 8
rs63750570
MAPT
0.827 0.120 17 46018629 missense variant G/A snv 8
rs35801418
LRRK2
0.827 0.120 12 40321114 missense variant A/G snv 7
rs63750376
MAPT
0.827 0.120 17 45996657 missense variant G/T snv 7
rs63751068
PSEN1
0.827 0.120 14 73186920 missense variant G/C;T snv 6
rs766001707
ATXN3
0.851 0.200 14 92096772 missense variant C/T snv 6
rs2435200
MAPT
0.925 0.080 17 45994485 intron variant G/A snv 0.40 5
rs1178466848
PRNP
0.925 0.120 20 4699785 missense variant G/A snv 2.8E-05 4
rs119467003
TDP1
0.882 0.080 14 89993420 missense variant A/G snv 2.1E-05 4
rs66468541
HSPD1
0.925 0.080 2 197497275 missense variant C/T snv 4
rs104893922
SMN1 ; SMN2
0.925 0.080 5 70946157 missense variant A/G snv 3
rs1272951905
MTHFSD
0.925 0.160 16 86532210 missense variant C/T snv 2.1E-05 3