Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs549908
IL18
0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29 10
rs4252019
IL1RN
0.882 0.160 2 113131542 intron variant C/T snv 0.25 3
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs33996649
PTPN22 ; AP4B1-AS1
0.732 0.400 1 113852067 missense variant C/T snv 1.7E-02 1.6E-02 13
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs2737190 0.827 0.120 9 117701903 upstream gene variant G/A snv 0.52 6
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 15
rs1371329921
TLR4
0.925 0.080 9 117712993 stop gained C/T snv 4.0E-06 1.4E-05 2
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
rs7873784
TLR4
0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 11
rs1927906
TLR4
1.000 0.080 9 117717837 3 prime UTR variant T/C snv 0.20 1
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs12998782
MARCO
0.882 0.160 2 118967804 intron variant C/T snv 0.19 3
rs17009726
MARCO
1.000 0.080 2 118967884 intron variant A/G snv 1.0E-02 1
rs2278589
MARCO
1.000 0.080 2 118971300 intron variant G/A;C snv 1
rs17795618
MARCO
1.000 0.080 2 118973892 intron variant T/A snv 0.12 1
rs1371562
MARCO
1.000 0.080 2 118975372 intron variant G/T snv 0.33 1
rs6761637
MARCO
1.000 0.080 2 118981487 missense variant T/C snv 8.3E-02 0.13 1
rs6751745
MARCO
0.925 0.080 2 118983428 intron variant C/T snv 0.31 2
rs2011839
MARCO
1.000 0.080 2 118985008 intron variant C/A;T snv 1
rs2522137
MSI1
0.827 0.120 12 120342128 3 prime UTR variant T/A;C;G snv 7
rs2393799
P2RX7 ; LOC105370032
0.882 0.200 12 121132209 upstream gene variant C/A;T snv 3
rs656612
P2RX7 ; LOC105370032
1.000 0.080 12 121138849 intron variant C/A snv 0.60 1