Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 1
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 1
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 3
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 1
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 1
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 2