Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1553510492
TBR1
2 161419040 missense variant A/G snv 4
rs9983925
ADARB1
21 45216929 intron variant C/T snv 0.46 4
rs10509125
ANK3
10 60167108 intron variant C/A snv 0.56 2
rs1799920
HTR1A
5 63961656 missense variant C/G;T snv 3.2E-04 2
rs1799921
HTR1A
5 63961638 missense variant T/C snv 9.4E-03 9.3E-03 2
rs200754713
PSEN2
1 226888954 missense variant A/G snv 4.0E-06; 4.0E-06 2
rs2049161
DLGAP1
18 4127583 intron variant A/C;T snv 0.22 2
rs279827
GABRA2
4 46332685 splice region variant A/G;T snv 0.44 0.41 2
rs35369693
AVPR1B
1 206116696 missense variant C/G;T snv 4.3E-02 2
rs1466835565
HK1
10 69368539 missense variant A/G snv 1
rs754747375
HK1
10 69369252 missense variant A/G snv 8.0E-06 7.0E-06 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59