Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs76151636 0.776 0.280 13 51944145 missense variant G/A;T snv 4.0E-06; 9.2E-04 10
rs5030849
PAH
0.851 0.280 12 102852875 missense variant C/A;G;T snv 2.2E-04 6
rs5030858
PAH
0.882 0.160 12 102840493 missense variant G/A snv 7.6E-04 9.0E-04 4
rs199475663
PAH
0.925 0.120 12 102866641 missense variant C/G;T snv 2.0E-05 3
rs5030841
PAH
0.925 0.120 12 102912816 missense variant A/G snv 1.2E-04 2.0E-04 3
rs5030851
PAH
0.925 0.160 12 102852815 missense variant G/A snv 1.0E-04 1.3E-04 3
rs5030853
PAH
0.925 0.120 12 102851701 missense variant C/A snv 5.9E-04 3.4E-04 3
rs5030856
PAH
0.925 0.120 12 102843676 missense variant T/C snv 9.9E-05 7.7E-05 3
rs5030860
PAH
0.925 0.120 12 102840474 missense variant T/C snv 3.7E-04 2.4E-04 3
rs62508588
PAH
1.000 0.120 12 102852929 missense variant C/A;T snv 7.6E-05 3
rs62514903
PAH
0.925 0.120 12 102894812 missense variant G/A snv 4.0E-06 1.4E-05 3
rs62642937
PAH
0.925 0.120 12 102843706 missense variant G/A snv 4.4E-04 3.6E-04 3
rs62644499
PAH
0.925 0.120 12 102840472 missense variant C/T snv 1.1E-04 1.1E-04 3
rs75193786
PAH
0.925 0.120 12 102894893 missense variant A/C;G;T snv 2.7E-04 3
rs76212747
PAH
0.925 0.120 12 102852923 missense variant A/G;T snv 4.8E-04; 2.4E-05 3
rs76687508
PAH
0.925 0.120 12 102852936 missense variant G/A snv 1.4E-04 8.4E-05 3
rs796052017
PAH
0.925 0.120 12 102852922 missense variant CA/TG mnv 3
rs1445893088
PAH
1.000 0.120 12 102840468 missense variant G/T snv 4.0E-06 2
rs199475567
PAH
1.000 0.120 12 102912791 missense variant C/A;T snv 2
rs199475572
PAH
1.000 0.120 12 102877475 missense variant T/A;C snv 2
rs199475658
PAH
1.000 0.120 12 102843646 missense variant C/G;T snv 4.0E-06 2
rs5030843
PAH
1.000 0.120 12 102866632 missense variant C/G;T snv 8.0E-06; 9.2E-05 2
rs5030846
PAH
1.000 0.120 12 102852930 stop gained G/A snv 4.4E-05 4.2E-05 2
rs5030847
PAH
1.000 0.120 12 102852903 missense variant G/A;C;T snv 2.8E-05; 4.0E-06 2
rs5030859
PAH
1.000 0.120 12 102840492 missense variant C/T snv 4.8E-05 3.5E-05 2