Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2274273 0.882 0.120 14 55147918 downstream gene variant G/A snv 0.40 5
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs17477177 1.000 0.080 7 106771412 upstream gene variant T/C snv 0.17 4
rs4779614 1.000 0.080 15 33247916 upstream gene variant T/C snv 0.72 1
rs4897549 1.000 0.080 6 131898350 upstream gene variant C/T snv 0.30 1
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs16933090 0.790 0.160 11 16434247 5 prime UTR variant C/T snv 0.12 7
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs371237692
REN
0.925 0.120 1 204159515 synonymous variant A/G snv 8.0E-06 3.5E-05 5
rs7439293 0.807 0.080 4 168756335 non coding transcript exon variant G/A snv 0.44 6
rs28357094 0.882 0.160 4 87975645 non coding transcript exon variant T/G snv 0.17 3
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
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
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
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99