Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2234591
WT1
0.925 0.080 11 32399873 intron variant T/C snv 1.4E-03 2
rs11212495
CUL5
1.000 11 108048172 intron variant A/G;T snv 1
rs1291142
SAMHD1
1.000 20 36896959 intron variant A/G;T snv 1
rs2294367
APOBEC3G
1.000 22 39083569 intron variant C/A;G snv 1
rs3736685
APOBEC3G
1.000 22 39081386 intron variant T/C snv 0.14 1
rs6001417
APOBEC3G
1.000 22 39081372 intron variant C/G snv 0.14 1
rs7103534
CUL5
1.000 11 108040925 intron variant T/C snv 0.13 1
rs11790131
LOC105375988
0.882 0.080 9 19469848 intergenic variant G/A;T snv 6
rs73084982
LOC105372508
0.882 0.080 20 3430406 intergenic variant G/A snv 3.5E-02 6
rs13064773 0.925 3 158893105 intergenic variant G/A snv 0.39 5
rs6594357 0.925 5 109205522 intergenic variant T/A;C snv 5
rs6723162 0.925 2 70875156 intergenic variant A/T snv 0.65 5
rs7458938 0.925 7 125820594 intergenic variant G/A snv 0.72 5
rs7576600
LOC105374497
0.925 2 40840846 intergenic variant C/A;G snv 5
rs30388
MAF
0.925 16 79580219 regulatory region variant T/C;G snv 5
rs147879075
CCR5 ; CCR5AS
1.000 3 46373902 stop gained C/A;G;T snv 1.6E-05; 8.2E-06; 4.1E-06 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs3775291
TLR3
0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs8177374
TIRAP
0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 11
rs241447
TAP2
0.827 0.280 6 32828974 missense variant T/C snv 0.31 0.26 11
rs1800451
MBL2
0.776 0.240 10 52771466 missense variant C/T snv 3.2E-02 7.9E-02 9