Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
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
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs333
CCR5 ; CCR5AS
0.667 0.520 3 46373453 frameshift variant GTCAGTATCAATTCTGGAAGAATTTCCAGACA/- delins 7.3E-02 23
rs1800630
TNF ; LOC100287329 ; LTA
0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs80338962
SCN4A
0.742 0.240 17 63941508 missense variant T/C snv 13
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 7
rs6596473
SLC23A1
0.807 0.120 5 139374887 intron variant G/C;T snv 7
rs3218977
IL1R2
0.807 0.240 2 102024739 3 prime UTR variant A/G snv 0.14 6
rs496892
CDKN2B-AS1
0.827 0.160 9 22024352 intron variant C/T snv 0.40 6
rs35068180
MMP3
0.851 0.040 11 102845217 upstream gene variant A/-;AA delins 5
rs1342913
BRINP3
0.851 0.040 1 190151895 intron variant G/A snv 0.61 4
rs1537415
GLT6D1
0.851 0.040 9 135637876 intron variant G/C snv 0.36 4
rs2981573
IL20
0.882 0.160 1 206867232 intron variant G/A snv 0.77 4
rs6667202
IL19
0.882 0.120 1 206783747 intron variant C/A;T snv 4
rs13005285
ATG16L1
0.882 0.080 2 233286311 intron variant T/G snv 0.56 3
rs1935881
BRINP3
0.882 0.080 1 190097256 downstream gene variant T/C snv 0.28 3
rs2679895
TGFBRAP1
0.882 0.080 2 105290023 intron variant C/A;G snv 3
rs3795391
S100A8
0.882 0.040 1 153390629 non coding transcript exon variant T/C snv 8.3E-02 3
rs3806232
S100A8
0.882 0.040 1 153391654 upstream gene variant T/C snv 0.15 3
rs1247559
LOC105378091
0.925 0.040 6 160782724 intron variant C/T snv 0.17 2
rs3218974
IL1R2
0.925 0.040 2 102024409 intron variant A/G snv 0.27 2