Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10925019
NLRP3
0.925 0.040 1 247432548 intron variant C/T snv 0.11 2
rs10951982
RAC1
0.851 0.160 7 6382925 intron variant G/A;T snv 5
rs10975003 0.882 0.080 9 5213687 intergenic variant T/C snv 0.43 3
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 8
rs11010067 0.925 0.040 10 35006503 downstream gene variant C/G snv 0.37 3
rs11054935
DUSP16
1.000 0.040 12 12495909 intron variant A/G snv 0.22 1
rs11064881
CIT
1.000 0.040 12 119709120 intron variant G/A snv 5.0E-02 3
rs11083840
PTGIR
1.000 0.040 19 46616653 downstream gene variant T/G snv 0.44 1
rs11098964
ANTXR2
0.827 0.120 4 79966815 intron variant A/G;T snv 5
rs11117431 0.807 0.160 16 85981710 intron variant A/G snv 0.18 6
rs111305875 0.827 0.120 6 167098098 intron variant T/G snv 3.0E-02 5
rs11133504 1.000 0.040 4 57514156 intergenic variant G/A snv 0.23 1
rs111456533
EEF1AKMT2
1.000 0.040 10 124750812 intron variant G/A snv 0.18 2
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs11150589
ITGAL
1.000 0.040 16 30471173 upstream gene variant T/A;C;G snv 2
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 9
rs11190133 0.827 0.120 10 99518968 intergenic variant C/T snv 0.26 5
rs11190140
NKX2-3 ; LINC01475
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 6
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs11221322
ETS1
0.827 0.120 11 128476898 intron variant T/C snv 0.13 5
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs11229555
GLYAT
0.827 0.120 11 58641214 intron variant G/T snv 0.21 7
rs11230563
LOC105369326 ; CD6
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 8