Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
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
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs10490924 0.716 0.240 10 122454932 missense variant G/T snv 0.26 0.23 16
rs11200638 0.724 0.280 10 122461028 non coding transcript exon variant G/A snv 0.23 14
rs1927914 0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52 14
rs2146323 0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs1048709 0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85 8
rs1136287 0.790 0.280 17 1769982 missense variant C/T snv 0.61 0.69 8
rs833069 0.851 0.200 6 43774842 non coding transcript exon variant T/C;G snv 5
rs9913583 0.925 0.120 17 1762036 5 prime UTR variant C/A snv 6.6E-02 2