Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10754558
NLRP3
0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 3
rs1077773
KCCAT333
1.000 0.040 7 17403055 intron variant G/A;C snv 2
rs10781499
CARD9
0.925 0.040 9 136371953 synonymous variant G/A snv 0.41 0.38 3
rs10797432
LOC100996583
1.000 0.040 1 2569899 downstream gene variant C/T snv 0.51 2
rs10798069
PLA2G4A
1.000 0.040 1 186906327 intron variant G/T snv 0.37 2
rs10800309 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 3
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs10896794
LPXN
11 58571651 intron variant T/C snv 0.19 1
rs10951982
RAC1
0.851 0.160 7 6382925 intron variant G/A;T snv 5
rs10956252
LOC105375746
8 125523895 intron variant C/G;T snv 1
rs11010067 0.925 0.040 10 35006503 downstream gene variant C/G snv 0.37 3
rs11064881
CIT
1.000 0.040 12 119709120 intron variant G/A snv 5.0E-02 3
rs111033623
SH2D1A ; STAG2
0.925 0.080 X 124365786 stop gained C/T snv 3
rs111456533
EEF1AKMT2
1.000 0.040 10 124750812 intron variant G/A snv 0.18 2
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
rs11187157 10 92742487 TF binding site variant T/C snv 0.40 1
rs11190140
NKX2-3 ; LINC01475
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 6
rs11195128 1.000 0.040 10 110426390 downstream gene variant C/G;T snv 2
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
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