Disease: Autism Spectrum Disorders
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10951154
HOTAIRM1 ; HOXA1
0.925 0.040 7 27095695 missense variant C/A;G;T snv 0.76 2
rs112795301
FOXP1
0.776 0.160 3 70972634 stop gained G/A snv 13
rs121917893
NLGN3
0.807 0.160 X 71167508 missense variant C/T snv 10
rs167771
DRD3
0.827 0.280 3 114157428 intron variant G/A;T snv 5
rs1800561
CD38
0.807 0.240 4 15824935 missense variant C/A;T snv 8.0E-06; 4.4E-04 7
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 12
rs2736654
GLO1
0.882 0.120 6 38682852 missense variant T/A;G snv 4
rs34808376 0.925 0.040 7 155456016 intron variant -/GC delins 2
rs362691
RELN
0.882 0.120 7 103610714 missense variant G/A;C;T snv 1.2E-05; 0.12 3
rs3735653
EN2
0.925 0.040 7 155458738 missense variant C/G;T snv 0.54 2
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
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 5
rs4746
GLO1
0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
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
rs779867
GRM7
0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1460808228
PRKCB
0.851 0.040 16 24185518 missense variant T/C snv 7.0E-06 4
rs201551401
GPR37
0.925 0.040 7 124746694 missense variant C/T snv 6.4E-05 1.4E-05 3