Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs62508613
PAH
0.925 0.120 12 102843629 intron variant C/T snv 7.0E-06 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
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
rs5030857
PAH
0.925 0.120 12 102840507 missense variant G/A snv 6.0E-04 5.6E-04 3
rs5030860
PAH
0.925 0.120 12 102840474 missense variant T/C snv 3.7E-04 2.4E-04 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
rs763115697
PAH
0.925 0.120 12 102846930 missense variant C/A;G;T snv 4.0E-06 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
rs104894275
PTS
0.882 0.120 11 112228665 missense variant A/G snv 1.2E-04 7.0E-06 3
rs104894276
PTS
0.882 0.120 11 112233178 missense variant C/G;T snv 4.0E-06; 7.6E-05 3
rs104894443 0.925 0.120 14 54844137 missense variant C/T snv 2
rs118092776
PAH
0.925 0.120 12 102912801 missense variant C/T snv 1.7E-03 9.2E-04 2
rs118203925
PAH
0.925 0.120 12 102912819 missense variant G/A;T snv 4.0E-06 2
rs199475598
PAH
0.925 0.120 12 102912794 missense variant A/C snv 1.7E-04 2.2E-04 2
rs199475602
PAH
0.925 0.120 12 102855313 missense variant C/G;T snv 2.0E-05; 1.6E-05 2
rs62507347
PAH
0.925 0.120 12 102894860 missense variant T/C;G snv 2