Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13000344 0.925 0.040 2 63062599 downstream gene variant T/G snv 0.11 2
rs1409313
CUEDC2
1.000 0.040 10 102431844 intron variant T/C snv 0.85 2
rs155806
PCDHA5 ; PCDHA7 ; PCDHA1 ; PCDHAC1 ; PCDHA10 ; PCDHA6 ; PCDHA11 ; PCDHAC2 ; PCDHA12 ; PCDHA13 ; PCDHA4 ; PCDHA9 ; PCDHA3 ; PCDHA2 ; PCDHA8
1.000 0.040 5 140970255 intron variant A/G snv 8.9E-02 2
rs1559619762
FOXP1
1.000 0.040 3 70977827 splice donor variant C/G snv 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
rs1882260
NLGN4X
1.000 0.040 X 5890820 3 prime UTR variant G/A snv 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
rs2351299
GABRB1
1.000 0.040 4 47141348 intron variant G/T snv 0.19 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
rs301434
SLC1A1 ; SPATA6L
0.925 0.040 9 4582082 intron variant C/G;T snv 2
rs301979
SPATA6L ; SLC1A1
0.925 0.040 9 4576851 intron variant G/A;C snv 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
rs3832300
GABRB1
1.000 0.040 4 47426318 3 prime UTR variant -/T delins 5.1E-02 2
rs4482737
GABRB1
1.000 0.040 4 47320173 missense variant T/C;G snv 0.99; 4.0E-06 2
rs4773054 1.000 0.040 13 109501681 intron variant T/C snv 0.89 2