Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs2072633 0.807 0.320 6 31951801 3 prime UTR variant A/G snv 0.59 6
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs57137919 0.776 0.160 21 42218908 intron variant G/A snv 0.14 9
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs767830104 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs5888 0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06 11
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs5985 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42