Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs541069027
CCR5 ; CCR5AS
1.000 3 46373290 missense variant G/A snv 1.8E-04 4.2E-05 1
rs184279915
CCR5AS ; CCR5
1.000 3 46373708 missense variant G/A;T snv 3.2E-05; 1.2E-05 1
rs1015164
CCRL2
0.925 3 46410189 intron variant A/C;G;T snv 8
rs17038463
CNTN6
0.925 3 1383484 intron variant T/C;G snv 5
rs777521033
CSF1
1.000 1 109923705 missense variant G/A;T snv 8.0E-06 1
rs11212495
CUL5
1.000 11 108048172 intron variant A/G;T snv 1
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
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs781172058
CXCR4
0.732 0.320 2 136115340 synonymous variant C/T snv 4.0E-06 16
rs10808739
CYP7B1
0.882 8 64727703 intron variant G/A snv 0.24 6
rs749701046
DNAH8
1.000 6 38723032 missense variant G/A snv 4.1E-06 1
rs12460243
FBN3
0.925 19 8066356 intron variant G/A snv 0.14 5
rs17691394
GRM8
0.925 7 126684537 intron variant A/G snv 0.13 5
rs4704846
HAVCR2
1.000 5 157086333 3 prime UTR variant G/A snv 0.79 2
rs2442719
HLA-B
0.882 0.120 6 31352761 intron variant C/T snv 0.53 6
rs1063320
HLA-G
0.752 0.360 6 29830972 3 prime UTR variant C/G;T snv 12
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs368234815
IFNL4
0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs35897606
KIAA1549L
0.882 0.080 11 33436311 intron variant A/G snv 4.4E-02 6
rs17169
LINC00298 ; LINC00299
0.925 2 8037334 intron variant G/T snv 0.13 5
rs79709413
LOC105370118
0.882 0.080 13 24740488 upstream gene variant G/T snv 4.7E-02 6