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
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1799793
ERCC2
0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs28934908
MECP2
0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 23
rs121917893
NLGN3
0.807 0.160 X 71167508 missense variant C/T snv 10
rs397514679
SYN1
0.790 0.200 X 47574321 stop gained G/A snv 9
rs6323
MAOA
0.807 0.040 X 43731789 synonymous variant G/T snv 0.65 7
rs1414334
HTR2C
0.851 0.160 X 114903581 intron variant C/G snv 5
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 5
rs779545541
GPHN
0.882 0.120 14 66965293 missense variant C/T snv 4.0E-06 5
rs3027407
MAOA
0.925 0.040 X 43745594 3 prime UTR variant A/G snv 3
rs3747333
NLGN4X
0.925 0.040 X 5893491 missense variant G/A;C;T snv 7.6E-03 3
rs3747334
NLGN4X
0.925 0.040 X 5893489 synonymous variant G/A;C;T snv 1.2E-05; 6.7E-03 3
rs587777457
MAOA
0.925 0.200 X 43731695 missense variant G/T snv 3
rs750257282
CARS1 ; CARS1-AS1
1.000 0.040 11 3038127 missense variant C/G;T snv 3.2E-05 3
rs768913131
NRXN1
0.925 0.040 2 50552821 missense variant G/A snv 3
rs1163276899
CACNA1D
1.000 0.040 3 53673125 missense variant G/A snv 2
rs1275980031
RELN
1.000 0.040 7 103540259 missense variant G/A snv 4.0E-06 2
rs1350135
FOXP2
1.000 0.040 7 114602621 intron variant C/A;G;T snv 2
rs1801291
MAOA
1.000 0.040 X 43744144 synonymous variant T/C snv 2
rs199473391
CACNA1C
1.000 0.040 12 2607117 stop gained G/A;T snv 2
rs4541
CYP11B1 ; GML
1.000 0.040 8 142875277 missense variant G/A;T snv 7.8E-02; 2.0E-05 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs201551401
GPR37
0.925 0.040 7 124746694 missense variant C/T snv 6.4E-05 1.4E-05 3