Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs515299
CFH
0.925 0.080 1 196737547 missense variant G/A;C;T snv 4.8E-05; 1.7E-02 4
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs4897081 0.882 0.160 6 149115402 upstream gene variant G/A;T snv 3
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4821480
MYH9
0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs4819554
IL17RA
0.776 0.320 22 17084145 upstream gene variant G/A snv 0.84 10
rs4730751
CAV1
0.882 0.120 7 116540796 intron variant C/A snv 0.22 4
rs4714384
EDN1
0.925 0.080 6 12297620 downstream gene variant T/C snv 0.45 2
rs4586
CCL2
0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48 8
rs4553808
CTLA4
0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs452204
IL1RN
0.807 0.200 2 113131484 intron variant G/A snv 0.45 7
rs4281481
CCDC179 ; GAS2
0.882 0.080 11 22859013 intron variant C/G snv 0.36 3
rs4253373
KLKB1
0.925 0.080 4 186250250 missense variant C/A snv 6.7E-04 2.5E-03 2
rs41302867
RREB1
0.925 0.080 6 7240643 intron variant G/A snv 8.5E-02 8.2E-02 3
rs398123538
IQCB1
0.882 0.200 3 121772605 frameshift variant TG/- delins 8.0E-05 7.0E-05 6
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs3957357
GSTA1
0.807 0.280 6 52803889 upstream gene variant A/G snv 0.63 7
rs3803800
TNFSF13 ; TNFSF12-TNFSF13
0.807 0.240 17 7559652 missense variant A/G snv 0.70 0.64 7
rs379489
CFH
0.851 0.200 1 196724321 intron variant A/G snv 0.65 4
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs3760106
PRKCB
0.925 0.080 16 23834475 upstream gene variant C/T snv 0.23 3
rs3759126
AQP2
0.882 0.080 12 49950079 upstream gene variant A/G snv 0.23 3