Disease: Autism Spectrum Disorders
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13000344 0.925 0.040 2 63062599 downstream gene variant T/G snv 0.11 2
rs34808376 0.925 0.040 7 155456016 intron variant -/GC delins 2
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 5
rs6150410 0.925 0.040 7 155454910 intron variant CGCATCCCC/-;CGCATCCCCCGCATCCCC delins 0.28 2
rs73598374
ADA
0.790 0.280 20 44651586 missense variant C/A;G;T snv 7.1E-06; 6.2E-02 8
rs35424709
ATP13A4
0.925 0.040 3 193454190 missense variant T/A snv 8.6E-02 7.8E-02 2
rs2278556
ATP2B2
0.925 0.040 3 10360419 intron variant G/A snv 0.34 2
rs35678
ATP2B2
0.925 0.040 3 10338239 missense variant C/T snv 0.49 0.47 2
rs10877969
AVPR1A
0.882 0.120 12 63153459 intron variant T/C snv 0.26 6
rs7294536
AVPR1A
0.925 0.040 12 63154312 upstream gene variant T/C snv 0.26 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs25925
CAMK4
0.925 0.040 5 111484055 synonymous variant G/C snv 0.75 0.83 2
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs2268498
CAV3 ; OXTR
0.827 0.080 3 8770725 intron variant T/C snv 0.41 7
rs237889
CAV3 ; OXTR
0.925 0.040 3 8760797 intron variant T/C snv 0.71 2
rs1800561
CD38
0.807 0.240 4 15824935 missense variant C/A;T snv 8.0E-06; 4.4E-04 7
rs3796863
CD38
0.790 0.160 4 15848363 intron variant G/T snv 0.41 8
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 12
rs7794745
CNTNAP2
0.851 0.040 7 146792514 intron variant A/T snv 0.49 6
rs7170637
CYFIP1
0.925 0.040 15 22903836 missense variant C/T snv 0.18 0.30 2
rs747756965
DNAH8
0.925 0.040 6 38775924 missense variant T/A;C snv 4.0E-06 2
rs7608798
DPP4
0.925 0.040 2 162033707 intron variant G/A snv 0.35 2
rs167771
DRD3
0.827 0.280 3 114157428 intron variant G/A;T snv 5
rs10498676
ELOVL2
0.925 0.040 6 11026766 intron variant G/A snv 0.18 3
rs1861972
EN2
0.925 0.040 7 155461298 intron variant G/A snv 0.72 2