Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9804190
ANK3
0.882 0.040 10 60080073 intron variant C/T snv 0.30 5
rs2144025
ESR1
0.925 0.080 6 151986571 intron variant T/A;C snv 4
rs279826
GABRA2
1.000 0.080 4 46332192 intron variant A/G snv 0.46 4
rs4916723
LINC00461
0.925 0.040 5 88558577 intron variant A/C;G;T snv 4
rs9983925
ADARB1
21 45216929 intron variant C/T snv 0.46 4
rs2074898
NDUFS7
1.000 0.040 19 1391362 intron variant A/C;G snv 3
rs3915512
DLG1 ; MIR4797
1.000 0.040 3 197295369 intron variant A/G;T snv 3
rs10509125
ANK3
10 60167108 intron variant C/A snv 0.56 2
rs2049161
DLGAP1
18 4127583 intron variant A/C;T snv 0.22 2
rs142441643
SDHA
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04 15
rs1060503383
SYNGAP1
0.882 0.200 6 33441318 stop gained C/T snv 14
rs886041097
NAA15
0.882 0.160 4 139386152 stop gained C/G snv 9
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
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42