Disease: Autism Spectrum Disorders
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs13000344 0.925 0.040 2 63062599 downstream gene variant T/G snv 0.11 2
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
rs2292813
SLC25A12
0.882 0.040 2 171787719 intron variant T/C snv 0.81 3
rs6735330
XPO1
0.925 0.040 2 61504343 intron variant G/A snv 0.18 2
rs7608798
DPP4
0.925 0.040 2 162033707 intron variant G/A snv 0.35 2
rs768913131
NRXN1
0.925 0.040 2 50552821 missense variant G/A snv 3
rs112795301
FOXP1
0.776 0.160 3 70972634 stop gained G/A snv 13
rs167771
DRD3
0.827 0.280 3 114157428 intron variant G/A;T snv 5
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
rs237889
CAV3 ; OXTR
0.925 0.040 3 8760797 intron variant T/C snv 0.71 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
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs779867
GRM7
0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs1800561
CD38
0.807 0.240 4 15824935 missense variant C/A;T snv 8.0E-06; 4.4E-04 7
rs1912960
GABRA4
0.925 0.040 4 46951864 intron variant G/C snv 0.28 2
rs3796863
CD38
0.790 0.160 4 15848363 intron variant G/T snv 0.41 8
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs25925
CAMK4
0.925 0.040 5 111484055 synonymous variant G/C snv 0.75 0.83 2