Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11689958
ADAM17
0.925 0.080 2 9557277 upstream gene variant G/A snv 0.19 2
rs41279766
MARCO
0.925 0.080 2 118970217 missense variant C/G;T snv 2.1E-03 2
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs1043210477
GPX1
0.701 0.520 3 49358250 missense variant G/A snv 19
rs1129055
CD86
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 15
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs17281995
CD86
0.763 0.360 3 122120794 3 prime UTR variant G/A;C snv 11
rs414171
MAPKAPK3 ; CISH
0.790 0.200 3 50612068 5 prime UTR variant A/G;T snv 9
rs17036188
PPARG
0.882 0.120 3 12299426 intron variant T/C snv 4.0E-02 3
rs2972164
PPARG
0.925 0.080 3 12292917 intron variant T/C snv 0.46 3
rs352162 0.882 0.160 3 52218953 non coding transcript exon variant T/C snv 0.55 3
rs4684846
PPARG
0.882 0.080 3 12297350 intron variant A/G snv 0.28 3
rs1153879
STAG1
0.925 0.080 3 136392816 intron variant G/T snv 2
rs1915087
CD86
0.925 0.080 3 122119944 3 prime UTR variant T/C snv 2
rs2332096
CD86
0.925 0.080 3 122102296 intron variant T/A;G snv 2
rs2715267
ILDR1
0.925 0.080 3 122052011 upstream gene variant G/A;T snv 2
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs121917864
TLR2
0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs5743551
TLR1
0.742 0.240 4 38806033 intron variant T/A;C snv 12
rs12508721
IL21-AS1
0.742 0.360 4 122623509 intron variant C/T snv 0.24 11
rs4648068
NFKB1
0.790 0.240 4 102597148 intron variant A/G snv 0.31 9