Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075277
P2RX6
1.000 0.120 22 21028193 3 prime UTR variant T/C snv 0.19 1
rs17004598
RRP1B ; HSF2BP
1.000 0.120 21 43658675 intron variant T/G snv 4.5E-02 1
rs3815700
ANKRD27
1.000 0.120 19 32602346 intron variant T/C snv 0.19 1
rs9956738
DCC
1.000 0.120 18 52414603 intron variant A/G snv 4.6E-02 1
rs3744790
CEP295NL ; TIMP2
1.000 0.120 17 78897053 intron variant C/T snv 0.14 1
rs12924112
CLEC16A
1.000 0.120 16 11125863 intron variant T/A;G snv 1
rs371915
MEAK7
1.000 0.120 16 84544635 intron variant A/C;G;T snv 1
rs8041227 1.000 0.120 15 31246339 intergenic variant G/A snv 0.18 1
rs8008716
LINC02588
1.000 0.120 14 26656559 intron variant A/G snv 8.9E-02 1
rs324011
STAT6
0.742 0.360 12 57108399 intron variant C/T snv 0.32 12
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs167769
STAT6
0.827 0.280 12 57109992 5 prime UTR variant C/T snv 0.31 5
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
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
rs118086209
CCDC81
1.000 0.120 11 86393453 intron variant T/C;G snv 1
rs77301713
CAPN5
1.000 0.120 11 77121400 intron variant G/A snv 2.0E-02 1
rs11819199 1.000 0.120 10 20576228 intergenic variant A/G snv 0.12 1
rs2898261
XKR6
1.000 0.120 8 11101029 intron variant G/A;T snv 1
rs11495981
JAZF1
1.000 0.120 7 28137682 intron variant C/T snv 0.29 2
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 13
rs599707 0.925 0.200 6 31840659 downstream gene variant C/T snv 7.6E-02 2
rs3806933
TSLP
0.807 0.360 5 111071044 5 prime UTR variant C/A;T snv 0.40 7
rs2416257
WDR36
0.882 0.160 5 111099792 intron variant C/G;T snv 5
rs3806932
TSLP
0.925 0.160 5 111069977 upstream gene variant A/G snv 0.51 3