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
rs777521033
CSF1
1.000 1 109923705 missense variant G/A;T snv 8.0E-06 1
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs371074389
LOC112268426 ; CXCR4
0.732 0.320 2 136115226 synonymous variant C/T snv 4.0E-06 4.2E-05 16
rs766914563
LOC112268426 ; CXCR4
0.732 0.320 2 136115082 synonymous variant C/T snv 7.0E-06 16
rs781172058
CXCR4
0.732 0.320 2 136115340 synonymous variant C/T snv 4.0E-06 16
rs17169
LINC00298 ; LINC00299
0.925 2 8037334 intron variant G/T snv 0.13 5
rs6542826
SH3RF3 ; RANBP2
0.925 2 109433263 intron variant A/G snv 0.51 5
rs6723162 0.925 2 70875156 intergenic variant A/T snv 0.65 5
rs7576600
LOC105374497
0.925 2 40840846 intergenic variant C/A;G snv 5
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 11
rs1015164
CCRL2
0.925 3 46410189 intron variant A/C;G;T snv 8
rs1126477
LTF
0.807 0.200 3 46459778 missense variant C/T snv 0.34 0.53 7
rs73132848
CAV3 ; OXTR
0.882 0.080 3 8764738 intron variant G/A snv 9.3E-02 6
rs13064773 0.925 3 158893105 intergenic variant G/A snv 0.39 5
rs16823858 0.925 3 115559835 intron variant G/A;C snv 5
rs17038463
CNTN6
0.925 3 1383484 intron variant T/C;G snv 5
rs183662584
CCR5 ; CCR5AS
1.000 3 46373218 missense variant G/A snv 5.2E-04 1.5E-04 2
rs147879075
CCR5 ; CCR5AS
1.000 3 46373902 stop gained C/A;G;T snv 1.6E-05; 8.2E-06; 4.1E-06 1
rs184279915
CCR5AS ; CCR5
1.000 3 46373708 missense variant G/A;T snv 3.2E-05; 1.2E-05 1
rs541069027
CCR5 ; CCR5AS
1.000 3 46373290 missense variant G/A snv 1.8E-04 4.2E-05 1
rs3775291
TLR3
0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs4835796
REEP2
0.925 5 138446426 3 prime UTR variant T/G snv 0.56 5