Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9533156
TNFSF11
0.807 0.280 13 42573535 intron variant T/C snv 0.47 8
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs7873784
TLR4
0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 11
rs7762544 0.882 0.040 6 41411577 intergenic variant G/A snv 0.81 3
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs73318382
MIR3142HG
1.000 0.040 5 160467536 intron variant A/C snv 5.4E-02 1
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs689466
PACERR ; PTGS2
0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs6596473
SLC23A1
0.807 0.120 5 139374887 intron variant G/C;T snv 7
rs652438
MMP12
0.716 0.400 11 102865911 missense variant T/C;G snv 7.1E-02; 2.5E-04 14
rs650108
MMP3
0.827 0.160 11 102838056 intron variant G/A snv 0.31 6
rs639752
WTAPP1 ; MMP3
0.882 0.120 11 102836608 non coding transcript exon variant C/A snv 0.54 3
rs6354
SLC6A4
0.732 0.280 17 30222880 5 prime UTR variant G/C;T snv 16
rs61752717
MEFV
0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs5906435
SYN1
1.000 0.040 X 47589011 intron variant C/G;T snv 1
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223