Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17125721
PSEN1
0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs104893875
SNCA
0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs104894201
CRYAB
0.763 0.280 11 111908934 missense variant T/C snv 12
rs3173615
TMEM106B
0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 12
rs104893768
RHO
0.807 0.080 3 129528801 missense variant C/A snv 11
rs398122403
SYNJ1
0.807 0.080 21 32695106 missense variant C/T snv 1.2E-05 11
rs121909329
VCP
0.763 0.200 9 35065363 missense variant C/A;G;T snv 11
rs1424266770
CASP3
0.790 0.200 4 184632307 missense variant C/G snv 8.0E-06 10
rs5030732
UCHL1 ; UCHL1-AS1
0.790 0.160 4 41257616 missense variant C/A snv 0.24 0.16 10
rs431905511
SNCA
0.827 0.080 4 89828154 missense variant C/T snv 9
rs121909715
GSN
0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 8
rs34015634
LRRK2
0.851 0.120 12 40340380 missense variant T/C snv 3.2E-05 1.4E-05 8
rs1052553
MAPT
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 8
rs63750570
MAPT
0.827 0.120 17 46018629 missense variant G/A snv 8
rs63750311
PSEN1
0.790 0.240 14 73192647 missense variant A/C snv 8
rs755221106
CACNA1G
0.851 0.040 17 50617560 missense variant G/A;T snv 4.0E-06 7
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
rs121912442
SOD1 ; LOC102724449
0.807 0.120 21 31659783 missense variant C/T snv 3.6E-05 7
rs766001707
ATXN3
0.851 0.200 14 92096772 missense variant C/T snv 6
rs75548401
GBA
0.882 0.160 1 155236246 missense variant G/A snv 5.9E-03 6.2E-03 6
rs63751294
GRN
0.827 0.120 17 44352404 stop gained C/T snv 8.0E-06 6
rs587777606
HNRNPUL2-BSCL2 ; BSCL2 ; LRRN4CL
0.851 0.160 11 62691300 stop gained G/A snv 4.0E-06 7.0E-06 6
rs63750869
MAPT
0.827 0.160 17 46018707 missense variant G/A snv 2.4E-05 5.6E-05 6
rs9468
MAPT
0.882 0.080 17 46024197 3 prime UTR variant T/C snv 0.15 0.14 6