Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6021191
NFATC2
0.851 0.120 20 51419700 intron variant A/T snv 4.9E-02 5
rs6479778
ARID5B
0.827 0.200 10 61929318 intron variant T/C;G snv 5
rs1057519773
ABL1
0.851 0.160 9 130872901 missense variant T/A;C;G snv 4
rs121913451
ABL1
0.851 0.160 9 130872903 missense variant C/A;G snv 4
rs17007695 0.851 0.120 4 141788570 intergenic variant T/C snv 7.7E-02 4
rs186364861
NUDT15 ; SUCLA2
0.882 0.120 13 48037798 missense variant G/A snv 9.1E-04 2.4E-04 4
rs2274407
ABCC4
0.882 0.120 13 95206781 missense variant C/A;G;T snv 9.7E-02 0.10 4
rs4748793 0.851 0.120 10 22194082 intergenic variant A/G snv 0.18 4
rs6964969
IKZF1
0.851 0.120 7 50405553 downstream gene variant A/G snv 0.23 4
rs7073837
ARID5B
0.851 0.120 10 61940136 intron variant A/C snv 0.58 0.64 4
rs7088318
PIP4K2A
0.851 0.120 10 22564019 intron variant C/A snv 0.55 4
rs766639320
CLTA
0.851 0.240 9 36211617 missense variant C/G snv 4.0E-06 4
rs121909646
FLT3
0.882 0.120 13 28018504 missense variant T/A;G snv 3
rs12540874
GRB10
0.882 0.280 7 50597225 intron variant A/C;G snv 3
rs12669559
IKZF1
1.000 0.120 7 50368079 synonymous variant T/G snv 0.35 0.32 3
rs12786200
FAT3
1.000 0.120 11 92245852 intergenic variant C/T snv 0.22 3
rs144104656 1.000 0.120 2 118661291 regulatory region variant A/G snv 1.1E-03 3
rs147481775
DEPDC5
1.000 0.120 22 31829377 intron variant C/A snv 6.6E-03 3
rs149940960
GREB1
1.000 0.120 2 11641492 3 prime UTR variant T/C snv 1.0E-02 3
rs17032980 1.000 0.120 2 67075611 intergenic variant A/G snv 0.25 3
rs34531324
LINC01411
1.000 0.120 5 174435441 intron variant A/T snv 0.16 3
rs3781093
GATA3
0.882 0.120 10 8059964 intron variant T/C snv 0.19 3
rs3794845
MBP
0.882 0.120 18 77002561 intron variant G/C snv 0.12 3
rs41307935
ZDHHC18
1.000 0.120 1 26854576 3 prime UTR variant C/T snv 6.1E-02 3
rs4245555
GRB10
1.000 0.120 7 50593712 intron variant T/C snv 0.32 3