Disease: Sepsis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs867186
PROCR ; MMP24-AS1-EDEM2
0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 15
rs5743551
TLR1
0.742 0.240 4 38806033 intron variant T/A;C snv 12
rs2234246
TREM1
0.827 0.240 6 41276002 3 prime UTR variant C/T snv 0.44 5
rs2234237
TREM1
0.763 0.280 6 41282728 missense variant T/A snv 0.13 0.12 9
rs2839693
CXCL12
0.882 0.120 10 44379119 intron variant T/A;C snv 3
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64