Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7103534
CUL5
1.000 11 108040925 intron variant T/C snv 0.13 1
rs7117111
CUL5
1.000 11 108046360 synonymous variant A/G snv 0.68 0.59 1
rs11212495
CUL5
1.000 11 108048172 intron variant A/G;T snv 1
rs6594357 0.925 5 109205522 intergenic variant T/A;C snv 5
rs6542826
SH3RF3 ; RANBP2
0.925 2 109433263 intron variant A/G snv 0.51 5
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
rs16823858 0.925 3 115559835 intron variant G/A;C snv 5
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
rs10892324
SLC37A4
0.925 11 119032329 upstream gene variant T/A;G snv 5
rs1406795590
TMED2
1.000 12 123586856 missense variant G/A snv 1
rs7458938 0.925 7 125820594 intergenic variant G/A snv 0.72 5
rs8177374
TIRAP
0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs17691394
GRM8
0.925 7 126684537 intron variant A/G snv 0.13 5
rs143633948
ARG1
0.882 0.080 6 131504454 intron variant G/A;C snv 6
rs11649112
LOC107984137 ; SHISA9
0.925 16 13267554 intron variant G/A snv 0.22 5
rs766914563
LOC112268426 ; CXCR4
0.732 0.320 2 136115082 synonymous variant C/T snv 7.0E-06 16
rs371074389
LOC112268426 ; CXCR4
0.732 0.320 2 136115226 synonymous variant C/T snv 4.0E-06 4.2E-05 16
rs781172058
CXCR4
0.732 0.320 2 136115340 synonymous variant C/T snv 4.0E-06 16
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs17038463
CNTN6
0.925 3 1383484 intron variant T/C;G snv 5
rs4835796
REEP2
0.925 5 138446426 3 prime UTR variant T/G snv 0.56 5
rs4704846
HAVCR2
1.000 5 157086333 3 prime UTR variant G/A snv 0.79 2
rs13064773 0.925 3 158893105 intergenic variant G/A snv 0.39 5