Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6944602 0.925 0.120 7 50406053 downstream gene variant G/A;T snv 1
rs10821938
ARID5B
0.925 0.120 10 61965014 intron variant A/C snv 0.56 1
rs199695765
CPA2
0.925 0.160 7 130269008 stop gained C/T snv 8.8E-05 1.3E-04 1
rs2242041
FIGNL1 ; DDC
0.925 0.120 7 50461751 intron variant C/G snv 7.7E-02 1
rs121913232
FLT3
0.925 0.120 13 28018500 missense variant G/C snv 1
rs12540874
GRB10
0.882 0.280 7 50597225 intron variant A/C;G snv 1
rs7896246
ARID5B
0.925 0.120 10 61964631 intron variant A/G snv 0.74 2
rs408626
DHFR ; MSH3
0.925 0.120 5 80655314 non coding transcript exon variant T/C snv 0.48 2
rs1339159756
INSL6 ; JAK2
0.925 0.120 9 5078395 missense variant C/G snv 2
rs78380171
LOC101927518
0.925 0.120 3 86720838 intergenic variant A/G snv 6.6E-03 2
rs442767
MSH3 ; DHFR
0.925 0.120 5 80655677 intron variant G/T snv 0.27 2
rs147390019
NUDT15
0.925 0.120 13 48045720 missense variant G/A snv 2.6E-03 2.2E-03 2
rs17007695 0.851 0.120 4 141788570 intergenic variant T/C snv 7.7E-02 3
rs4748793 0.851 0.120 10 22194082 intergenic variant A/G snv 0.18 3
rs7073837
ARID5B
0.851 0.120 10 61940136 intron variant A/C snv 0.58 0.64 3
rs6964969
IKZF1
0.851 0.120 7 50405553 downstream gene variant A/G snv 0.23 3
rs3794845
MBP
0.882 0.120 18 77002561 intron variant G/C snv 0.12 3
rs7088318
PIP4K2A
0.851 0.120 10 22564019 intron variant C/A snv 0.55 3
rs2274407
ABCC4
0.882 0.120 13 95206781 missense variant C/A;G;T snv 9.7E-02 0.10 4
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
rs766639320
CLTA
0.851 0.240 9 36211617 missense variant C/G snv 4.0E-06 4
rs2036914
F11
0.882 0.160 4 186271327 intron variant T/C snv 0.57 4
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 4
rs6021191
NFATC2
0.851 0.120 20 51419700 intron variant A/T snv 4.9E-02 4