Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs12190287 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs76863441 0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs375752214 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs7493 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113