Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6323
MAOA
0.807 0.040 X 43731789 synonymous variant G/T snv 0.65 7
rs736707
LOC101927870 ; RELN
0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs7794745
CNTNAP2
0.851 0.040 7 146792514 intron variant A/T snv 0.49 6
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs13316193
CAV3 ; OXTR
0.882 0.040 3 8761057 intron variant T/C snv 0.45 4
rs1452075
CADPS
1.000 0.040 3 62495388 intron variant C/T snv 0.73 4
rs1460808228
PRKCB
0.851 0.040 16 24185518 missense variant T/C snv 7.0E-06 4
rs1858830
MET
0.925 0.040 7 116672385 5 prime UTR variant C/G snv 0.40 4
rs2056202
SLC25A12
0.882 0.040 2 171855970 intron variant T/C snv 0.81 0.77 4
rs6551665
ADGRL3
0.882 0.040 4 61873823 intron variant G/A snv 0.59 4
rs1042778
CAV3 ; OXTR
0.925 0.040 3 8752859 3 prime UTR variant G/A;C;T snv 3
rs10498676
ELOVL2
0.925 0.040 6 11026766 intron variant G/A snv 0.18 3
rs201551401
GPR37
0.925 0.040 7 124746694 missense variant C/T snv 6.4E-05 1.4E-05 3
rs2268493
CAV3 ; OXTR
0.882 0.040 3 8759154 intron variant T/C snv 0.25 3
rs2292813
SLC25A12
0.882 0.040 2 171787719 intron variant T/C snv 0.81 3
rs237902
CAV3 ; OXTR
0.925 0.040 3 8767498 synonymous variant G/A snv 0.29 0.31 3
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
rs4141463
MACROD2
0.925 0.040 20 14766825 intron variant T/C snv 0.50 3
rs526126
FADS2
1.000 0.040 11 61857413 intron variant G/C;T snv 0.81; 8.0E-06 3
rs6565113
CDH13
0.925 0.040 16 83074041 intron variant G/C;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
rs10230087
FOXP2
1.000 0.040 7 114614352 intron variant G/A snv 0.73 2