Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs310241
JAK1
0.882 0.360 1 64837655 intron variant A/G snv 0.37 3
rs1044573
ENTPD6
0.925 0.120 20 25226018 3 prime UTR variant A/G snv 0.49 2
rs11466749
TSLP
0.925 0.120 5 111076887 3 prime UTR variant A/G snv 0.15 2
rs13395467
LINC00299
1.000 0.120 2 8311368 intron variant A/G snv 0.24 2
rs148505069 1.000 0.120 4 122496409 intergenic variant A/G snv 0.29 2
rs1892280 0.925 0.120 6 52192184 downstream gene variant A/G snv 0.60 2
rs34004019
HLA-DQB1-AS1
1.000 0.120 6 32658626 upstream gene variant A/G snv 0.29 2
rs3787184
NFATC2
1.000 0.120 20 51541298 intron variant A/G snv 0.17 2
rs61977073
TTC6
1.000 0.120 14 37682050 intron variant A/G snv 0.16 2
rs6898653 0.925 0.120 5 116639960 intergenic variant A/G snv 0.26 2
rs111371454
RTF1
1.000 0.120 15 41468419 intron variant A/G snv 0.34 1
rs2297377
RPAP1
1.000 0.120 15 41523451 intron variant A/G snv 0.44 1
rs2823048 1.000 0.120 21 15089947 intergenic variant A/G snv 0.18 1
rs2823053 1.000 0.120 21 15092828 intergenic variant A/G snv 0.27 1
rs4713039
SYCP2L
1.000 0.120 6 10906023 synonymous variant A/G snv 0.20 0.15 1
rs7824993 1.000 0.120 8 80350661 intron variant A/G snv 0.62 1
rs9282864
SULT1A1
1.000 0.120 16 28605987 intron variant A/G snv 0.34 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4794820
LRRC3C
0.790 0.160 17 39933091 intron variant A/G;T snv 9
rs438421
IL12RB1
0.882 0.200 19 18065276 intron variant A/G;T snv 3
rs10124907 1.000 0.120 9 25659639 intergenic variant A/G;T snv 1
rs2884670
DYRK4
1.000 0.120 12 4566052 intron variant A/G;T snv 1
rs1479430148
VEGFA
1.000 0.120 6 43784861 3 prime UTR variant A/T snv 1
rs74604924
HRH4
1.000 0.120 18 24477515 stop gained A/T snv 1
rs7780001 1.000 0.120 7 19438358 intron variant A/T snv 0.17 1