Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs2296147 0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs4353229 0.807 0.160 10 113729830 3 prime UTR variant T/C snv 0.23 6
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs121912470 0.925 0.120 5 132489448 missense variant A/G snv 2
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55