Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs1429638 0.925 0.080 4 73872213 downstream gene variant C/A;G snv 0.17 2
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs353291
CARMN ; MIR145
0.807 0.200 5 149431183 non coding transcript exon variant T/C snv 0.35 6
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5
rs2563298
TMCO6 ; CD14
0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26 4
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
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
rs510432
ATG5
0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs2234237
TREM1
0.763 0.280 6 41282728 missense variant T/A snv 0.13 0.12 9
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 8
rs2234246
TREM1
0.827 0.240 6 41276002 3 prime UTR variant C/T snv 0.44 5
rs1554162524
ELOVL4
0.882 0.160 6 79925034 splice acceptor variant T/C snv 4
rs805305
DDAH2
0.882 0.120 6 31729610 intron variant C/G snv 0.48 3
rs506027
ATG5
0.925 0.080 6 106326589 upstream gene variant G/A snv 0.57 2
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246