Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
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
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs4673
CYBA
0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs33939927
LRRK2
0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs63750756
MAPT
0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs63750306
PSEN1
0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs80356537
ATP1A3
0.752 0.320 19 41970405 missense variant C/A;G;T snv 17
rs63750082
PSEN1
0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs28936379
PSEN2
0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs371425292
APP
0.763 0.160 21 25897627 missense variant C/A;T snv 8.0E-06 10
rs1386984902
APP
0.790 0.160 21 26000095 missense variant G/A snv 9
rs387906709
UBQLN2
0.776 0.120 X 56565363 missense variant C/A;T snv 9
rs121909668
FUS
0.790 0.120 16 31191418 missense variant C/A;G;T snv 1.2E-05 8
rs77369218
GBA
0.807 0.160 1 155235726 missense variant T/A snv 7
rs1329650
HECTD2-AS1
0.882 0.080 10 91588363 regulatory region variant G/A;T snv 6
rs2189814
GRM3
0.925 0.040 7 86702440 intron variant T/A;C snv 3
rs761715536
ADRA2A
1.000 0.040 10 111079092 stop gained G/A;T snv 6.4E-06; 1.3E-05 3
rs1245342105
SPTBN1
1.000 0.040 2 54622367 missense variant T/C snv 4.0E-06 2
rs1223904774
APP
0.790 0.120 21 25891772 missense variant C/T snv 4.0E-06 7.0E-06 8
rs1315695444
SELP
1.000 0.040 1 169611580 missense variant C/G snv 4.0E-06 1.4E-05 2