Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7073837
ARID5B
0.851 0.120 10 61940136 intron variant A/C snv 0.58 0.64 4
rs74709575
LINC02334
1.000 0.120 13 38041119 intron variant A/C snv 3.1E-03 3
rs10821938
ARID5B
0.925 0.120 10 61965014 intron variant A/C snv 0.56 2
rs8015478
CEBPE
1.000 0.120 14 23116809 downstream gene variant A/C snv 0.68 2
rs7923074
ARID5B
1.000 0.120 10 61963681 intron variant A/C snv 0.56 1
rs12540874
GRB10
0.882 0.280 7 50597225 intron variant A/C;G snv 3
rs4617118
CCDC26
1.000 0.120 8 129143897 intron variant A/C;G snv 0.20 1
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs17855750
IL27
0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21
rs3731217
CDKN2A
0.763 0.320 9 21984662 intron variant A/C;T snv 10
rs121913487
FLT3
0.925 0.120 13 28018503 missense variant A/C;T snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1801265
DPYD
0.763 0.280 1 97883329 missense variant A/G snv 0.28 13
rs11978267
IKZF1
0.763 0.240 7 50398606 intron variant A/G snv 0.25 9
rs1966862
ARHGAP24
0.790 0.120 4 85766908 intron variant A/G snv 0.14 8
rs10994982
ARID5B
0.790 0.120 10 61950345 intron variant A/G snv 0.49 7
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
rs144104656 1.000 0.120 2 118661291 regulatory region variant A/G snv 1.1E-03 3
rs17032980 1.000 0.120 2 67075611 intergenic variant A/G snv 0.25 3
rs11155133
LOC102723724
0.925 0.200 6 140848688 intron variant A/G snv 8.5E-02 2
rs78380171
LOC101927518
0.925 0.120 3 86720838 intergenic variant A/G snv 6.6E-03 2
rs7896246
ARID5B
0.925 0.120 10 61964631 intron variant A/G snv 0.74 2