Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs255012 1.000 0.200 7 41189487 regulatory region variant T/A;C snv 2
rs1364926780
ABCB1
0.882 0.200 7 87550272 missense variant C/T snv 5
rs199516560
ABCB1
0.851 0.200 7 87600772 5 prime UTR variant G/A snv 2.1E-05 5
rs1404008939
ABCB1
0.925 0.200 7 87504324 missense variant A/C;G snv 4.0E-06 4
rs3740066
ABCC2
0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20
rs2273697
ABCC2
0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 11
rs730882213
ADAT3 ; SCAMP4
0.925 0.080 19 1912477 missense variant G/A snv 7.0E-06 4
rs1445362103
ARHGEF7
1.000 0.040 13 111244248 missense variant T/C snv 1.2E-05 7.0E-06 2
rs1378981995
ARL13B
0.925 0.200 3 94003751 missense variant G/A snv 7.0E-06 3
rs122460151
ARSL
0.851 0.280 X 2958423 missense variant C/G snv 7.1E-05 3.8E-05 5
rs104894743
ARX
0.807 0.200 X 25012937 missense variant G/A snv 7
rs121918822
ASMT
Y 1642868 missense variant C/T snv 1
rs387907281
ATP1A3
0.752 0.280 19 41970284 missense variant C/T snv 13
rs587776690
ATR
0.882 0.280 3 142556439 synonymous variant T/C snv 4
rs1301785134
ATR
0.925 0.280 3 142556117 missense variant C/T snv 4.0E-06 3
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs180177035
BRAF
0.752 0.280 7 140801502 missense variant T/C snv 35
rs4846049
C1orf167 ; MTHFR
0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 11
rs118203933
CA2
0.925 0.360 8 85473779 missense variant C/T snv 8.0E-06 6
rs200115000
CAMK2B
1.000 0.160 7 44220165 missense variant C/A;G;T snv 2.6E-04; 5.8E-05 2
rs397514627
CAMK2G
0.882 0.160 10 73842486 missense variant C/A;G snv 5
rs10410239
CC2D1A
1.000 0.200 19 13919876 synonymous variant T/C snv 0.27 0.38 2
rs6511901
CC2D1A
1.000 0.200 19 13916839 intron variant C/T snv 0.39 2
rs753303079
CD55
1 207325673 missense variant C/G;T snv 8.0E-06 1