Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs36053993 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 31
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs4245739 0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 21
rs369410616 0.752 0.280 1 45329400 missense variant C/T snv 2.0E-05 2.8E-05 10
rs2274976 0.807 0.320 1 11790870 missense variant C/T snv 5.6E-02 4.2E-02 7
rs3768235 0.925 0.080 1 85267691 missense variant C/T snv 8.0E-06; 6.5E-02 4.5E-02 2
rs113998067 1.000 0.080 1 37607755 downstream gene variant T/C snv 3.3E-02 1
rs11583244 1.000 0.080 1 225764772 regulatory region variant C/T snv 0.35 1
rs79024726 1.000 0.080 1 33832760 intron variant T/A;G snv 1
rs819913 1.000 0.080 1 99299799 intron variant T/A;C snv 1
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1800440 0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs1056827 0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35 24
rs887829 0.763 0.280 2 233759924 intron variant C/T snv 0.36 18
rs10012 0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs2070959 0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 16
rs8175347 0.708 0.400 2 233760234 intron variant TATA/-;TA;TATATA;TATATATA;TATATATATA;TATATATATATA delins 16
rs63750875 0.742 0.280 2 47475171 missense variant G/A;C snv 1.6E-05 15
rs2072472 0.732 0.200 2 102026557 intron variant A/G snv 0.24 13
rs13405728 0.790 0.200 2 48751020 intron variant A/G snv 0.15 8