Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4958847
IRGM
0.807 0.120 5 150860025 intron variant G/A snv 0.25 8
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs540558
OSMR ; OSMR-AS1
0.925 0.120 5 38844171 intron variant C/G snv 0.19 2
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs6074028
CD40
1.000 0.040 20 46126219 intron variant A/C;G snv 1
rs61752717
MEFV
0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs7033979
ASPN ; CENPP
0.925 0.040 9 92461698 intron variant A/G;T snv 2
rs73115010
CD40
1.000 0.040 20 46124597 intron variant T/C snv 0.18 1
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs741761
SEMA7A ; MIR6881
0.882 0.200 15 74411588 missense variant T/A;C snv 1.8E-04; 0.35 3
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs771184127
NOD2
0.790 0.200 16 50710807 missense variant G/A snv 1.2E-05 2.1E-05 9
rs778767225
MOK
0.851 0.200 14 102231805 missense variant C/A snv 2.4E-05 7.0E-06 4
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 8
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14