Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs1800630
TNF ; LOC100287329 ; LTA
0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs7096206
MBL2
0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 10
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs4979462
TNFSF15
0.790 0.240 9 114804733 intron variant C/T snv 0.13 7
rs5746136
SOD2
0.807 0.200 6 159682052 3 prime UTR variant C/T snv 0.27 6
rs3753395
CFH
0.882 0.120 1 196717522 intron variant A/G;T snv 5
rs42490
RIPK2
0.882 0.160 8 89766285 intron variant G/A snv 0.60 5
rs7759127
HLA-B ; HLA-C
0.925 0.040 6 31273211 intron variant T/G snv 0.11 5
rs10114470
TNFSF15
0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 4
rs10905284
GATA3
0.882 0.200 10 8073399 intron variant C/A;T snv 4
rs1333955
PACRG
0.851 0.080 6 162792422 intron variant T/A;C snv 4
rs2058660
IL18RAP
0.882 0.280 2 102437989 intron variant G/A snv 0.78 4
rs3793964
TOLLIP
0.882 0.120 11 1280752 intron variant T/C snv 0.66 4
rs7194886 0.851 0.080 16 50691282 upstream gene variant C/T snv 0.38 4