Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11684747
ADAM17
0.925 0.080 2 9557042 upstream gene variant A/G snv 0.19 2
rs497116
CASP12
0.925 0.080 11 104892390 stop lost A/G snv 4.3E-02 2
rs8177375
TIRAP
0.925 0.080 11 126293169 3 prime UTR variant A/G snv 0.12 0.13 2
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs747126003
IL6-AS1 ; IL6
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06 18
rs414171
MAPKAPK3 ; CISH
0.790 0.200 3 50612068 5 prime UTR variant A/G;T snv 9
rs2027432
NLRP3
0.882 0.160 1 247415139 upstream gene variant A/G;T snv 3
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs13137
VMP1 ; MIR21
0.827 0.160 17 59841670 3 prime UTR variant A/T snv 0.18 5
rs9770242
NAMPT
0.851 0.240 7 106285885 5 prime UTR variant C/A snv 0.79 5
rs2563298
TMCO6 ; CD14
0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26 4
rs1429638 0.925 0.080 4 73872213 downstream gene variant C/A;G snv 0.17 2
rs4755453
TRAF6 ; RAG1
0.925 0.080 11 36509094 intron variant C/A;G;T snv 2
rs368287711
IL10RA
0.851 0.120 11 117989554 missense variant C/A;T snv 2.0E-05; 2.4E-05 4
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs4919510
SEMA4G ; MIR608 ; MRPL43
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs11465996
LY96
0.790 0.240 8 73989727 upstream gene variant C/G snv 0.25 7
rs805305
DDAH2
0.882 0.120 6 31729610 intron variant C/G snv 0.48 3