Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs768623239
GSTM1 ; GSTM2
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs1801265
DPYD
0.763 0.280 1 97883329 missense variant A/G snv 0.28 13
rs20551
EP300
0.752 0.320 22 41152004 missense variant A/G snv 0.31 0.23 10
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
rs3135388
HLA-DRA
0.807 0.240 6 32445274 downstream gene variant A/G snv 0.90 7
rs762613037
SLC19A1 ; COL18A1
0.790 0.160 21 45512196 missense variant A/G snv 2.1E-05 7.0E-06 7
rs9479
PML
0.851 0.120 15 74036235 3 prime UTR variant A/G snv 0.50 6
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
rs1296957097
CHEK2
0.882 0.120 22 28719401 missense variant A/G snv 3
rs138047632
LOC107987304 ; SLC19A1
0.882 0.120 21 45525860 missense variant A/G snv 2.4E-03 2.2E-03 3
rs7809758
DDC ; FIGNL1
0.882 0.120 7 50505635 intron variant A/G snv 0.36 3
rs880028
FIGNL1 ; DDC
0.882 0.120 7 50502438 intron variant A/G snv 0.21 3
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
rs79327197
HLA-DOA
1.000 0.120 6 33010635 upstream gene variant A/G snv 1.6E-02 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs4553808
CTLA4
0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs2790
TYMS ; ENOSF1
0.925 0.160 18 673086 3 prime UTR variant A/G;T snv 0.22 2