Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs6136
SELP
0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1805094
LEPR
0.716 0.440 1 65610269 missense variant G/C;T snv 0.16; 4.0E-06 16
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs5355
C1orf112 ; SELE
0.742 0.240 1 169726729 missense variant G/A snv 4.5E-02 3.3E-02 14
rs5744174
TLR5
0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs6330
NGF ; NGF-AS1
0.763 0.240 1 115286692 missense variant G/A snv 0.37 0.36 12
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 11
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 11
rs4612666
NLRP3
0.763 0.440 1 247435768 intron variant T/C snv 0.65 10
rs4846048
MTHFR ; C1orf167
0.752 0.280 1 11786195 3 prime UTR variant G/A snv 0.67 10
rs2266780
FMO3
0.827 0.280 1 171114102 missense variant A/G snv 0.15 0.14 9
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
rs689470
PTGS2
0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv 9
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 8
rs2229569
SELL ; C1orf112
0.790 0.360 1 169704697 missense variant G/A;T snv 0.21; 3.2E-05 8
rs3021094
IL10 ; IL19
0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 8
rs9333025
CYP4A11
0.851 0.200 1 46931231 intron variant C/T snv 9.4E-02 8
rs1554286
IL19 ; IL10
0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72 7
rs1764391
SMIM12 ; GJA4 ; LOC105378642
0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 7
rs2266782
FMO3
0.851 0.200 1 171107825 missense variant G/A snv 0.37 0.41 7