Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs147377392 0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
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
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
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
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs884164 0.925 0.040 19 4521613 upstream gene variant A/G;T snv 2
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs5880 0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 10
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs7944926 0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs11234027 0.882 0.080 11 71523061 intron variant G/A snv 0.24 5
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147