Disease: Autism Spectrum Disorders
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10498676
ELOVL2
0.925 0.040 6 11026766 intron variant G/A snv 0.18 3
rs10877969
AVPR1A
0.882 0.120 12 63153459 intron variant T/C snv 0.26 6
rs1340513
KDM4C
0.882 0.120 9 6977633 intron variant G/A snv 0.75 4
rs167771
DRD3
0.827 0.280 3 114157428 intron variant G/A;T snv 5
rs16976358
LINC00907
0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 6
rs1861972
EN2
0.925 0.040 7 155461298 intron variant G/A snv 0.72 2
rs1861973
EN2
0.925 0.040 7 155461450 intron variant T/C snv 0.73 2
rs1881084
SND1
0.925 0.040 7 127704626 intron variant G/A snv 0.33 2
rs1912960
GABRA4
0.925 0.040 4 46951864 intron variant G/C snv 0.28 2
rs2056202
SLC25A12
0.882 0.040 2 171855970 intron variant T/C snv 0.81 0.77 4
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
rs2278556
ATP2B2
0.925 0.040 3 10360419 intron variant G/A snv 0.34 2
rs2292813
SLC25A12
0.882 0.040 2 171787719 intron variant T/C snv 0.81 3
rs237889
CAV3 ; OXTR
0.925 0.040 3 8760797 intron variant T/C snv 0.71 2
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 12
rs2896218
WNT2
0.925 0.040 7 117279924 intron variant G/A snv 0.60 2
rs34808376 0.925 0.040 7 155456016 intron variant -/GC delins 2
rs3796863
CD38
0.790 0.160 4 15848363 intron variant G/T snv 0.41 8
rs4141463
MACROD2
0.925 0.040 20 14766825 intron variant T/C snv 0.50 3
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 5
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6150410 0.925 0.040 7 155454910 intron variant CGCATCCCC/-;CGCATCCCCCGCATCCCC delins 0.28 2
rs6735330
XPO1
0.925 0.040 2 61504343 intron variant G/A snv 0.18 2
rs6950765
WNT2
0.925 0.040 7 117281176 intron variant C/G snv 0.64 2