Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs7944926
NADSYN1
0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs35897606
KIAA1549L
0.882 0.080 11 33436311 intron variant A/G snv 4.4E-02 6
rs4074
CXCL1
0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs9275319 0.807 0.200 6 32698518 intergenic variant A/G snv 0.15 6
rs1475539937
TLR9
0.882 0.120 3 52223085 missense variant A/G snv 4.0E-06 5
rs11506105
EGFR
0.851 0.160 7 55152484 intron variant A/G snv 0.59 4
rs3194051
IL7R
0.851 0.200 5 35876172 missense variant A/G snv 0.24 0.28 4
rs7383287
HLA-DOB
0.851 0.320 6 32815309 synonymous variant A/G snv 0.18 0.19 4
rs868
TGFBR1
0.851 0.160 9 99149374 3 prime UTR variant A/G snv 0.17 4
rs11574129
VDR
0.882 0.160 12 47843520 3 prime UTR variant A/G snv 1.6E-02 3
rs11881222
IFNL3
0.925 0.080 19 39244283 intron variant A/G snv 0.30 3
rs1634323
TLR7
0.882 0.200 X 12870008 intron variant A/G snv 0.11 3
rs4619915
CXCL11 ; ART3
0.882 0.120 4 76034048 3 prime UTR variant A/G snv 0.61 3
rs538399
IGFBP4
0.925 0.120 17 40454413 intron variant A/G snv 0.33 3
rs730775
NFKBIE
1.000 0.080 6 44264337 intron variant A/G snv 0.36 3
rs760370
SLC29A1
0.925 0.120 6 44233216 intron variant A/G snv 0.36 3
rs1297986
LINC00636
1.000 0.080 3 107912675 intron variant A/G snv 2
rs2629751
GLT8D2
0.925 0.120 12 104028030 intron variant A/G snv 0.36 2
rs2856723 0.925 0.120 6 32699985 intergenic variant A/G snv 0.63 2
rs1029153
CXCL12
1.000 0.080 10 44371698 3 prime UTR variant A/G snv 0.27 1
rs1049807
LOC101927369 ; CCL4
1.000 0.080 17 36105270 missense variant A/G snv 0.22 0.21 1
rs1484994
BCL2L1
1.000 0.080 20 31718172 intron variant A/G snv 0.38 1
rs1997060
NLGN1
1.000 0.080 3 174035108 intron variant A/G snv 0.18 1
rs56378326
PKIB
1.000 0.080 6 122670278 intron variant A/G snv 2.6E-02 1