Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1020608562
CCR5AS ; CCR5
0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 11
rs11884476
PARD3B
2 205453869 intron variant C/G snv 0.11 1
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs1233579 0.925 0.160 6 28744886 intergenic variant A/G snv 7.2E-02 3
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs13194504 0.925 0.120 6 28662914 intergenic variant G/A snv 5.1E-02 3
rs1369619997
KIDINS220
2 8731746 missense variant G/C snv 4.0E-06 1
rs14158
LDLR
0.851 0.160 19 11131368 synonymous variant G/A snv 0.24 0.22 5
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
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 0.69 108
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs2284178
HCP5
0.925 0.120 6 31464348 non coding transcript exon variant C/T snv 0.44 6
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 12
rs241447
TAP2
0.827 0.280 6 32828974 missense variant T/C snv 0.31 0.26 11
rs2516509
MICB-DT
0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 10
rs2844513 0.925 0.120 6 31420437 intron variant G/A snv 0.53 6
rs2894207
LINC02571 ; HLA-B
0.882 0.160 6 31295974 intron variant T/C snv 0.20 8
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 9
rs3117143
LOC100129636
0.882 0.160 6 29063365 intron variant C/A snv 5.2E-02 4
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs3131093 0.925 0.160 6 28869660 intergenic variant C/T snv 7.1E-02 3
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48