Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs113994097
POLG
0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04 22
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs5569
SLC6A2
0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs143624519
MAPT
0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs113994099
POLG
0.827 0.240 15 89320883 missense variant T/C snv 10
rs63750756
MAPT
0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs367543041
TARDBP
0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs242557
MAPT
0.752 0.200 17 45942346 intron variant G/A snv 0.36 12
rs74315414
PRNP
0.882 0.200 20 4699533 missense variant C/A;T snv 4.0E-06 5
rs41549716
POLG
0.882 0.200 15 89321842 missense variant T/C snv 6.6E-03 7.0E-03 4
rs886039227
DCTN1
0.925 0.200 2 74378123 missense variant A/C snv 4
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 18
rs1555507479
GNAO1
0.807 0.160 16 56336799 missense variant C/A snv 12
rs188286943
VPS35
0.776 0.160 16 46662452 missense variant C/T snv 9
rs542171324
SNCA
0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 6
rs3135500
NOD2
0.851 0.160 16 50732975 3 prime UTR variant G/A snv 0.44 5