Disease: Autism Spectrum Disorders
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs7170637
CYFIP1
0.925 0.040 15 22903836 missense variant C/T snv 0.18 0.30 2
rs73598374
ADA
0.790 0.280 20 44651586 missense variant C/A;G;T snv 7.1E-06; 6.2E-02 8
rs747756965
DNAH8
0.925 0.040 6 38775924 missense variant T/A;C snv 4.0E-06 2
rs751945904
NLGN4X
0.925 0.040 X 5893158 missense variant G/A snv 1.1E-05 2
rs768913131
NRXN1
0.925 0.040 2 50552821 missense variant G/A snv 3
rs79667838
GRPR
0.882 0.120 X 16150432 missense variant C/T snv 3.0E-04 4.8E-04 3
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1060826
NOS2
0.851 0.160 17 27762841 synonymous variant T/C snv 0.66 0.67 4
rs25925
CAMK4
0.925 0.040 5 111484055 synonymous variant G/C snv 0.75 0.83 2
rs301430
SLC1A1 ; SPATA6L
0.827 0.080 9 4576680 synonymous variant T/C snv 0.36 0.38 7
rs3747334
NLGN4X
0.925 0.040 X 5893489 synonymous variant G/A;C;T snv 1.2E-05; 6.7E-03 3
rs1858830
MET
0.925 0.040 7 116672385 5 prime UTR variant C/G snv 0.40 4
rs1051312
SNAP25 ; SNAP25-AS1
0.827 0.120 20 10306440 3 prime UTR variant T/C snv 0.20 5
rs2018650
LOC100132215 ; EHBP1
0.925 0.040 2 63045589 3 prime UTR variant T/C snv 0.11 2
rs3746544
SNAP25 ; SNAP25-AS1
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs7294536
AVPR1A
0.925 0.040 12 63154312 upstream gene variant T/C snv 0.26 2
rs13000344 0.925 0.040 2 63062599 downstream gene variant T/G snv 0.11 2