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
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1554210073
PHIP
0.752 0.320 6 79042844 frameshift variant GT/A delins 21
rs5569
SLC6A2
0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs1131691771
PHIP ; IRAK1BP1
0.807 0.160 6 78958469 splice donor variant ACTT/- delins 18
rs1555565492
RAI1
0.776 0.160 17 17795417 frameshift variant -/G delins 18
rs1562150844
PHIP
0.790 0.280 6 78982908 frameshift variant CTTT/- delins 14
rs1135402761
SYT1
0.827 0.320 12 79448958 missense variant T/C snv 11
rs27072
SLC6A3
0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs75634836
HTR2A
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06 11
rs686
DRD1
0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs886041097
NAA15
0.882 0.160 4 139386152 stop gained C/G snv 9
rs1800955
DRD4
0.827 0.160 11 636784 upstream gene variant T/C;G snv 8
rs63750570
MAPT
0.827 0.120 17 46018629 missense variant G/A snv 8
rs3745406
PRKCG
0.851 0.080 19 53891711 missense variant T/A;C snv 4.0E-06; 0.41 6
rs1565922388
SYT1
0.925 12 79353599 missense variant T/A snv 5
rs1565922395
SYT1
0.925 12 79353602 missense variant A/G snv 5
rs1565962725
SYT1
0.925 12 79448953 missense variant C/A snv 5
rs265981
DRD1
0.925 0.080 5 175443899 5 prime UTR variant A/G;T snv 3
rs594242
HTR2A
1.000 0.040 13 46883917 intron variant C/A;G snv 3
rs1004212
NRXN3
14 78714883 synonymous variant C/G;T snv 8.0E-06; 0.15 2
rs806379
CNR1
1.000 0.040 6 88151548 intron variant A/C;T snv 2
rs144900171
SYT1
0.925 12 79448968 missense variant C/G;T snv 1.3E-04 6.2E-04 5
rs79874540
PSMD1 ; HTR2B
0.925 0.080 2 231123707 stop gained G/A snv 1.5E-03 1.2E-03 4
rs6736017
PSMD1 ; HTR2B
2 231108702 missense variant T/C snv 6.3E-03 2.5E-02 4