Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.463 0.714 6 26092913 missense variant G/A snp 3.3E-02 3.8E-02 175
rs397507444 0.457 0.714 1 11794407 missense variant T/G snp 169
rs1799945 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 152
rs4986790 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 146
rs1799983 0.475 0.786 7 150999023 missense variant T/A,G snp 0.75 0.76 138
rs4880 0.536 0.643 6 159692840 missense variant A/G snp 0.48 0.47 81
rs1801282 0.543 0.679 3 12351626 missense variant C/G snp 0.11 1.0E-01 77
rs1805192 0.545 0.679 3 12379739 missense variant C/G snp 75
rs5443 0.570 0.571 12 6845711 synonymous variant C/T snp 0.36 0.43 65
rs16139 0.657 0.500 7 24285260 missense variant T/A,C snp 4.0E-06; 3.0E-02 3.2E-02 27
rs696217 0.685 0.536 3 10289773 missense variant G/T snp 8.8E-02 7.2E-02 24
rs2241766 0.679 0.393 3 186853103 synonymous variant T/C,G snp 8.0E-06; 0.13 9.0E-02 23
rs11887534 0.685 0.357 2 43839108 missense variant G/A,C snp 6.4E-06; 6.7E-02 6.4E-02 20
rs5186 0.744 0.250 3 148742201 3 prime UTR variant A/C snp 0.23 0.20 14
rs1799752
ACE
0.756 0.286 17 63488529 intron variant T/TATACAGTCACTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCC,TG in-del 11
rs1044498 0.801 0.250 6 131851228 missense variant A/C,G snp 0.19 0.32 8
rs281432 0.821 0.250 19 10279982 intron variant C/G snp 0.51 6
rs743507 0.923 0.143 7 151010400 intron variant C/T snp 0.78 3