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
rs1051312
SNAP25 ; SNAP25-AS1
0.827 0.120 20 10306440 3 prime UTR variant T/C snv 0.20 5
rs1060826
NOS2
0.851 0.160 17 27762841 synonymous variant T/C snv 0.66 0.67 4
rs10877969
AVPR1A
0.882 0.120 12 63153459 intron variant T/C snv 0.26 6
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
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121917893
NLGN3
0.807 0.160 X 71167508 missense variant C/T snv 10
rs13000344 0.925 0.040 2 63062599 downstream gene variant T/G snv 0.11 2
rs1340513
KDM4C
0.882 0.120 9 6977633 intron variant G/A snv 0.75 4
rs1460808228
PRKCB
0.851 0.040 16 24185518 missense variant T/C snv 7.0E-06 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
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1800561
CD38
0.807 0.240 4 15824935 missense variant C/A;T snv 8.0E-06; 4.4E-04 7
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
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