Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1137100
LEPR
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs768623239
GSTM1 ; GSTM2
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs2735940
TERT
0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 25
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
rs34009635
MMP8
0.716 0.360 11 102713445 missense variant A/G snv 2.5E-03 6.2E-04 17
rs750521832
MMP8
0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06 14
rs1801265
DPYD
0.763 0.280 1 97883329 missense variant A/G snv 0.28 13
rs6218
LINC02456 ; HELLPAR ; IGF1
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs20551
EP300
0.752 0.320 22 41152004 missense variant A/G snv 0.31 0.23 10
rs3021097
IL10 ; IL19
0.752 0.440 1 206773289 5 prime UTR variant A/G snv 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
rs1164376164
ABCB1
0.851 0.200 7 87601024 5 prime UTR variant A/G snv 6
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
rs35837782
LHPP
0.925 0.120 10 124604740 intron variant A/G snv 0.63 2