Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 107
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 66
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 44
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs3732379
CX3CR1
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 32
rs767830104
CXCR4
0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs1020608562
CCR5AS ; CCR5
0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 6
rs241447
TAP2
0.827 0.280 6 32828974 missense variant T/C snv 0.31 0.26 6
rs14158
LDLR
0.851 0.160 19 11131368 synonymous variant G/A snv 0.24 0.22 5
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 5
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 4
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 3
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 3
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 2
rs2894207
LINC02571 ; HLA-B
0.882 0.160 6 31295974 intron variant T/C snv 0.20 2
rs919266
BST2
19 17403506 intron variant T/C;G snv 1
rs1369619997
KIDINS220
2 8731746 missense variant G/C snv 4.0E-06 1
rs374596032
KIDINS220
2 8813255 missense variant A/C;G snv 4.0E-06; 8.0E-06 1
rs9368699
SNHG32 ; SNORD48
0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 1
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 1