Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs7022797
C9orf47 ; S1PR3
0.882 0.120 9 88989548 upstream gene variant T/G snv 0.38 3
rs653765
ADAM10
0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45 10
rs374520012
LBP
0.882 0.120 20 38373994 missense variant T/C;G snv 8.0E-06; 4.0E-06 3
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs510432
ATG5
0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs121918094
TTR
0.827 0.280 18 31592921 missense variant T/C snv 8
rs353291
CARMN ; MIR145
0.807 0.200 5 149431183 non coding transcript exon variant T/C snv 0.35 6
rs2232618
LBP
0.851 0.160 20 38373117 missense variant T/C snv 9.2E-02 0.12 5
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5
rs1554162524
ELOVL4
0.882 0.160 6 79925034 splice acceptor variant T/C snv 4
rs2721068
FOXO1
0.882 0.160 13 40565575 intron variant T/C snv 0.38 4
rs10506481
MIR6502 ; IRAK3
0.882 0.080 12 66250331 3 prime UTR variant T/C snv 9.0E-02 3
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
rs1915087
CD86
0.925 0.080 3 122119944 3 prime UTR variant T/C snv 2
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2332096
CD86
0.925 0.080 3 122102296 intron variant T/A;G snv 2
rs5743551
TLR1
0.742 0.240 4 38806033 intron variant T/A;C snv 12
rs2839693
CXCL12
0.882 0.120 10 44379119 intron variant T/A;C snv 3
rs2234237
TREM1
0.763 0.280 6 41282728 missense variant T/A snv 0.13 0.12 9
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19