Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs4969170
LOC101928674
0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 11
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 10
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs1805011
IL4R
0.776 0.320 16 27362551 missense variant A/C;G;T snv 0.13; 1.2E-04; 3.6E-05 8
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs8076131
ORMDL3
0.790 0.200 17 39924659 intron variant G/A;C snv 11
rs121912633
TRPV4
0.790 0.240 12 109792396 missense variant C/A;T snv 4.0E-06 10
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs2075820
NOD1
0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 10
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 9
rs4794820
LRRC3C
0.790 0.160 17 39933091 intron variant A/G;T snv 9
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 9
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18 8
rs569108
MS4A2
0.790 0.200 11 60095631 missense variant A/G snv 4.7E-02 7.3E-02 8
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 8
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 7
rs12603332
LOC112268187 ; ORMDL3 ; LRRC3C
0.807 0.200 17 39926554 5 prime UTR variant T/C snv 0.49 7
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7