Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1917799 0.851 0.120 10 49542929 upstream gene variant A/C snv 0.25 4
rs2709800
NOD1
0.882 0.120 7 30473155 intron variant A/C snv 0.53 4
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs5744174
TLR5
0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs3024496
IL10
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43 6
rs2301756
PTPN11
0.851 0.120 12 112452972 intron variant A/G snv 0.21 4
rs718226
LOC102724907
0.882 0.120 16 50735652 intron variant A/G snv 0.36 4
rs10420321
DNMT1
0.925 0.080 19 10189741 intron variant A/G snv 0.11 2
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1550117
DNMT3A
0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs2015620
IL32
0.882 0.120 16 3073560 intron variant A/G;T snv 3
rs11536878
TLR4
0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02 5
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs2066842
NOD2
0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 15
rs3024491
IL19 ; IL10
0.925 0.040 1 206771701 intron variant C/A;T snv 2
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
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1179251
IL22 ; LOC105369818
0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs1640827
TLR5
0.882 0.120 1 223138265 intron variant C/G;T snv 3
rs7205423
LOC102724907
1.000 0.040 16 50735351 intron variant C/G;T snv 1
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34