Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 13
rs324011
STAT6
0.742 0.360 12 57108399 intron variant C/T snv 0.32 12
rs4671393
BCL11A
0.790 0.400 2 60493816 intron variant A/C;G snv 11
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs3806933
TSLP
0.807 0.360 5 111071044 5 prime UTR variant C/A;T snv 0.40 7
rs167769
STAT6
0.827 0.280 12 57109992 5 prime UTR variant C/T snv 0.31 5
rs2416257
WDR36
0.882 0.160 5 111099792 intron variant C/G;T snv 5
rs61894547
EMSY
0.882 0.160 11 76537586 intron variant C/T snv 3.1E-02 4
rs7482144
HBG2
0.882 0.280 11 5254939 3 prime UTR variant G/A snv 4
rs2296225
KIF17
0.882 0.160 1 20704549 missense variant T/C;G snv 0.12; 4.0E-06 3
rs1986734
SHROOM3
1.000 0.120 4 76499631 intron variant C/T snv 0.43 3
rs3806932
TSLP
0.925 0.160 5 111069977 upstream gene variant A/G snv 0.51 3
rs599707 0.925 0.200 6 31840659 downstream gene variant C/T snv 7.6E-02 2
rs489441
C5orf66
0.925 0.280 5 135158291 intron variant G/A;C;T snv 2
rs11495981
JAZF1
1.000 0.120 7 28137682 intron variant C/T snv 0.29 2
rs11819199 1.000 0.120 10 20576228 intergenic variant A/G snv 0.12 1
rs2000260 1.000 0.120 1 108130783 downstream gene variant A/G snv 0.37 1
rs2055376 1.000 0.120 5 116845732 regulatory region variant G/A;T snv 1
rs252716 1.000 0.120 5 111089365 intron variant G/A;C snv 1
rs6799767 1.000 0.120 3 176312308 intergenic variant G/A;T snv 1
rs8041227 1.000 0.120 15 31246339 intergenic variant G/A snv 0.18 1
rs3815700
ANKRD27
1.000 0.120 19 32602346 intron variant T/C snv 0.19 1
rs149864795
CAPN14
1.000 0.120 2 31179541 intron variant G/A snv 4.8E-02 1
rs6736278
CAPN14
1.000 0.120 2 31220009 intron variant C/T snv 5.4E-02 1