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
rs3918188 0.776 0.280 7 151005693 intron variant C/A;T snv 10
rs2228146 0.925 0.120 1 154454574 missense variant G/A snv 1.3E-02; 4.0E-06 5.4E-02 3
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
rs11915160 0.851 0.200 3 181713783 3 prime UTR variant C/A snv 0.11 5
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs17300539 0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs7756992 0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
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
rs751141 0.732 0.400 8 27516348 missense variant G/A snv 0.12 0.10 16
rs1137933 0.882 0.160 17 27778906 synonymous variant G/A snv 0.20 0.21 4