Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5
rs6586282
CBS
0.882 0.080 21 43058387 intron variant C/T snv 5
rs9770242
NAMPT
0.851 0.240 7 106285885 5 prime UTR variant C/A snv 0.79 5
rs1524668
ADAM17
0.851 0.160 2 9557243 upstream gene variant A/C snv 0.64 4
rs2563298
TMCO6 ; CD14
0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26 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
rs11137480
S1PR3 ; C9orf47
0.882 0.120 9 88989662 upstream gene variant G/C snv 0.37 3
rs12048215
NLRP3
0.882 0.160 1 247421289 intron variant A/G snv 0.11 3
rs17036188
PPARG
0.882 0.120 3 12299426 intron variant T/C snv 4.0E-02 3
rs2027432
NLRP3
0.882 0.160 1 247415139 upstream gene variant A/G;T snv 3
rs2839693
CXCL12
0.882 0.120 10 44379119 intron variant T/A;C snv 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
rs5743867
TOLLIP
0.882 0.120 11 1307121 intron variant G/A;C snv 3
rs7022797
C9orf47 ; S1PR3
0.882 0.120 9 88989548 upstream gene variant T/G snv 0.38 3
rs7119750
RELA
0.882 0.120 11 65655120 3 prime UTR variant C/G;T snv 3
rs805305
DDAH2
0.882 0.120 6 31729610 intron variant C/G snv 0.48 3
rs11216153
APOA1-AS
0.925 0.080 11 116834384 upstream gene variant G/T snv 0.16 2
rs1153879
STAG1
0.925 0.080 3 136392816 intron variant G/T snv 2
rs11666254
FPR2 ; FPR1
0.925 0.080 19 51759909 intron variant A/G snv 0.28 2
rs11684747
ADAM17
0.925 0.080 2 9557042 upstream gene variant A/G snv 0.19 2
rs11689958
ADAM17
0.925 0.080 2 9557277 upstream gene variant G/A snv 0.19 2
rs12605436
MIR187
0.925 0.080 18 35906684 upstream gene variant C/T snv 9.1E-02 2