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
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
rs1460808228
PRKCB
0.851 0.040 16 24185518 missense variant T/C snv 7.0E-06 4
rs1858830
MET
0.925 0.040 7 116672385 5 prime UTR variant C/G snv 0.40 4
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
rs201551401
GPR37
0.925 0.040 7 124746694 missense variant C/T snv 6.4E-05 1.4E-05 3
rs2018650
LOC100132215 ; EHBP1
0.925 0.040 2 63045589 3 prime UTR variant T/C snv 0.11 2
rs2056202
SLC25A12
0.882 0.040 2 171855970 intron variant T/C snv 0.81 0.77 4
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
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
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
rs4141463
MACROD2
0.925 0.040 20 14766825 intron variant T/C snv 0.50 3