Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs28934906
MECP2
0.716 0.320 X 154031355 missense variant G/A snv 46
rs80338796
RAF1
0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 37
rs180177035
BRAF
0.752 0.280 7 140801502 missense variant T/C snv 35
rs28934908
MECP2
0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 23
rs3740066
ABCC2
0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20
rs387906799
KIF1A
0.742 0.200 2 240788118 missense variant G/A snv 19
rs267607165
TUBB3
0.708 0.520 16 89935679 missense variant G/A;C snv 18
rs587777308
GABRA1
0.763 0.040 5 161873196 missense variant G/A snv 14
rs1554032789
NIPBL
0.925 0.160 5 37048547 missense variant T/A snv 13
rs387907281
ATP1A3
0.752 0.280 19 41970284 missense variant C/T snv 13
rs536289169
GSTM1 ; GSTM2
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 13
rs80338758
MED12
0.790 0.400 X 71127367 missense variant C/A;T snv 12
rs4846049
C1orf167 ; MTHFR
0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 11
rs796052676
KCNQ3
0.807 0.200 8 132180246 missense variant G/A snv 10
rs28934904
MECP2
0.776 0.200 X 154031431 missense variant G/A;C;T snv 9
rs774843232
PGAP2
0.851 0.080 11 3825024 missense variant G/A;C;T snv 8.0E-06; 3.6E-05; 1.2E-05 9
rs1057516085
KCNQ2
0.827 0.080 20 63444747 missense variant C/T snv 8
rs587777623
DEAF1
0.882 0.120 11 686986 missense variant G/A snv 4.0E-06 8
rs104894743
ARX
0.807 0.200 X 25012937 missense variant G/A snv 7
rs869312966
SCN8A
0.827 0.120 12 51806345 missense variant G/T snv 7
rs879255652
SCN8A
0.807 0.120 12 51790425 stop gained G/A;T snv 7
rs118203933
CA2
0.925 0.360 8 85473779 missense variant C/T snv 8.0E-06 6
rs121918524
PHF8
0.827 0.200 X 54011232 missense variant A/G snv 6