Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3811046
IL37
0.851 0.160 2 112913801 missense variant G/A;T snv 4.0E-06; 0.71 5
rs35068180
MMP3
0.851 0.040 11 102845217 upstream gene variant A/-;AA delins 5
rs4252120
PLG
0.827 0.080 6 160722576 intron variant T/C;G snv 0.21 5
rs1342913
BRINP3
0.851 0.040 1 190151895 intron variant G/A snv 0.61 4
rs1537415
GLT6D1
0.851 0.040 9 135637876 intron variant G/C snv 0.36 4
rs6667202
IL19
0.882 0.120 1 206783747 intron variant C/A;T snv 4
rs2981573
IL20
0.882 0.160 1 206867232 intron variant G/A snv 0.77 4
rs13005285
ATG16L1
0.882 0.080 2 233286311 intron variant T/G snv 0.56 3
rs1935881
BRINP3
0.882 0.080 1 190097256 downstream gene variant T/C snv 0.28 3
rs104894211
CTSC
0.882 0.120 11 88294358 missense variant T/C snv 1.2E-05 3
rs2070746
FPR1
0.882 0.040 19 51746449 synonymous variant G/T snv 0.34 0.30 3
rs3795391
S100A8
0.882 0.040 1 153390629 non coding transcript exon variant T/C snv 8.3E-02 3
rs3806232
S100A8
0.882 0.040 1 153391654 upstream gene variant T/C snv 0.15 3
rs2241879
SCARNA5 ; ATG16L1
0.882 0.080 2 233274822 intron variant G/A snv 0.45 0.44 3
rs2679895
TGFBRAP1
0.882 0.080 2 105290023 intron variant C/A;G snv 3
rs536714306
ADGRG6
0.925 0.040 6 142419955 missense variant G/A snv 9.2E-05 2.8E-05 2
rs142548867
EEFSEC
0.925 0.040 3 128264663 missense variant C/T snv 1.8E-03 6.8E-04 2
rs782383264
ELN
0.925 0.040 7 74051750 missense variant G/A snv 1.2E-05 2
rs2070745
FPR1
0.925 0.040 19 51746694 missense variant C/G;T snv 0.40; 1.2E-05 2
rs5030879
FPR1
0.925 0.040 19 51746647 synonymous variant G/A snv 2.8E-02 9.5E-02 2
rs5030880
FPR1
0.925 0.040 19 51746427 missense variant T/A snv 0.13 0.12 2
rs779229249
GPRC6A
0.925 0.040 6 116807037 missense variant A/G snv 4.0E-06 2
rs61815643
IL19
0.925 0.040 1 206782771 intron variant G/A;T snv 2
rs3218974
IL1R2
0.925 0.040 2 102024409 intron variant A/G snv 0.27 2
rs3819370
IL1R2
0.925 0.040 2 102016112 non coding transcript exon variant A/G snv 0.17 2