Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs1800888
ADRB2
0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs2069885
IL9
0.851 0.120 5 135892476 missense variant G/A;C snv 0.11 5
rs3138557
IFNG ; IFNG-AS1
0.851 0.080 12 68158711 intron variant CGAG/- delins 4
rs4543123
TLR1
0.882 0.080 4 38790903 non coding transcript exon variant A/G snv 0.32 4
rs1799962
IL9
0.925 0.080 5 135896167 upstream gene variant T/C;G snv 7.2E-02 3
rs757275190
NUP214
1.000 9 131129441 missense variant T/A snv 1