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
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
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
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
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
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
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
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62