Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs1085307993
GABRB2
0.716 0.440 5 161331056 missense variant C/T snv 53
rs1057519389
EBF3
0.695 0.400 10 129957324 missense variant C/A;G;T snv 46
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs201893408
TMEM67
0.695 0.480 8 93795970 missense variant T/A;C snv 8.0E-06; 1.5E-04 28
rs1554389088
CAMK2B
0.807 0.160 7 44243526 missense variant G/A snv 27
rs6471
CYP21A2
0.683 0.360 6 32040110 missense variant G/A;C;T snv 1.2E-05; 5.3E-03 24
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs138659167
DHCR7
0.807 0.320 11 71435840 splice acceptor variant C/A;G snv 5.6E-05; 3.9E-03 20
rs61750240
MECP2
0.752 0.240 X 154031020 stop gained G/A;C snv 5.5E-06 19
rs606231435
ATP1A3
0.827 0.240 19 41970539 missense variant C/T snv 18
rs387906702
SMC1A
0.807 0.200 X 53403635 missense variant A/G snv 16
rs104894094
CDKN2A
0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06 12
rs1064797245
ATP1A3
0.776 0.280 19 41970540 missense variant G/A snv 12
rs1135402761
SYT1
0.827 0.320 12 79448958 missense variant T/C snv 11
rs1554504663
RHOBTB2
0.851 0.080 8 23007627 missense variant G/A snv 11
rs775104326
CTNNB1
0.776 0.160 3 41224995 stop gained C/A;T snv 4.0E-06 10
rs397518483
RARB
0.851 0.120 3 25596428 missense variant C/A;T snv 9
rs80356529
OPA1
0.827 0.240 3 193643996 missense variant G/A;C snv 9
rs864309483
ADCY5
0.851 0.080 3 123352464 missense variant G/A snv 9
rs1554402092
CAMK2B
1.000 7 44254555 missense variant C/T snv 8
rs587777057
GNAO1
0.827 0.040 16 56336744 missense variant G/A snv 8
rs776095655
SLC2A1
0.827 0.160 1 42927684 missense variant C/A;T snv 4.0E-06 8
rs1554121872
CAMK2A
0.882 0.040 5 150250270 missense variant T/G snv 7