Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs374596032
KIDINS220
2 8813255 missense variant A/C;G snv 4.0E-06; 8.0E-06 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 9
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs1233579 0.925 0.160 6 28744886 intergenic variant A/G snv 7.2E-02 3
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 10
rs3117143
LOC100129636
0.882 0.160 6 29063365 intron variant C/A snv 5.2E-02 4
rs11884476
PARD3B
2 205453869 intron variant C/G snv 0.11 1
rs767830104
CXCR4
0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs3732379
CX3CR1
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 11
rs2284178
HCP5
0.925 0.120 6 31464348 non coding transcript exon variant C/T snv 0.44 6
rs3131093 0.925 0.160 6 28869660 intergenic variant C/T snv 7.1E-02 3
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs3815087
PSORS1C1
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25 8
rs3823418
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 0.23 8
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 8
rs2844513 0.925 0.120 6 31420437 intron variant G/A snv 0.53 6