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
rs13000344 0.925 0.040 2 63062599 downstream gene variant T/G snv 0.11 2
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
rs2018650
LOC100132215 ; EHBP1
0.925 0.040 2 63045589 3 prime UTR variant T/C snv 0.11 2
rs2278556
ATP2B2
0.925 0.040 3 10360419 intron variant G/A snv 0.34 2
rs237889
CAV3 ; OXTR
0.925 0.040 3 8760797 intron variant T/C snv 0.71 2
rs25925
CAMK4
0.925 0.040 5 111484055 synonymous variant G/C snv 0.75 0.83 2
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
rs35424709
ATP13A4
0.925 0.040 3 193454190 missense variant T/A snv 8.6E-02 7.8E-02 2
rs35678
ATP2B2
0.925 0.040 3 10338239 missense variant C/T snv 0.49 0.47 2
rs370911031
NCS1
0.925 0.040 9 130219801 missense variant G/A snv 1.5E-04 8.4E-05 2
rs3735653
EN2
0.925 0.040 7 155458738 missense variant C/G;T snv 0.54 2
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
rs7170637
CYFIP1
0.925 0.040 15 22903836 missense variant C/T snv 0.18 0.30 2
rs7294536
AVPR1A
0.925 0.040 12 63154312 upstream gene variant T/C snv 0.26 2
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
rs756472
MRTFB
0.925 0.040 16 14185624 intron variant G/A snv 0.24 2
rs7608798
DPP4
0.925 0.040 2 162033707 intron variant G/A snv 0.35 2