Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1569547876 1.000 X 77841252 stop gained G/A snv 4
rs373260156 1.000 X 77830825 missense variant T/C;G snv 1.2E-05 3
rs765191836 1.000 4 55367628 stop gained G/A;T snv 4.0E-06 3
rs398124349 1.000 0.080 16 5082648 missense variant C/T snv 2
rs794726944 1.000 0.080 16 5071998 missense variant A/G snv 4.6E-06 2
rs151319324 1.000 0.080 16 8847797 missense variant G/A;C snv 5.7E-04; 8.0E-06; 4.0E-06 1
rs199562225 1.000 0.080 16 8813047 stop gained C/T snv 2.4E-05 1
rs370434427 1.000 0.080 3 184245562 stop gained C/A;G;T snv 4.0E-06; 4.0E-06; 1.2E-05 1
rs373562040 1.000 4 102344566 missense variant C/A;T snv 6.4E-04 1
rs374928784 16 5082674 splice donor variant G/A snv 1.6E-05 1
rs387907202 1.000 16 70512280 stop gained C/A;T snv 1
rs387907203 1.000 16 70481062 missense variant A/C;G snv 4.0E-06 1
rs587777116 1.000 0.080 20 50942070 missense variant C/A snv 1.6E-05 1
rs752922461 16 5071864 stop gained C/A;G;T snv 8.6E-06; 4.3E-06; 2.6E-05 1
rs864309660 1.000 4 102267916 missense variant C/G snv 1
rs886037858 1.000 6 117707002 missense variant G/A snv 4.0E-06 1
rs863225089 1.000 0.080 2 74464919 missense variant C/T snv 7.0E-06 1
rs16835020 1.000 0.080 16 5084798 missense variant C/T snv 4.3E-06; 8.6E-06 7.0E-06 1
rs794727301 1.000 0.080 16 5073004 missense variant T/G snv 7.0E-06 2
rs398124348 1.000 0.080 16 5082565 missense variant C/T snv 4.0E-06 1.4E-05 2
rs752307253 4 55364274 splice region variant G/- del 3.2E-05 1.4E-05 1
rs794727073 16 5083680 splice acceptor variant A/G snv 2.1E-05 1
rs746019074 1.000 0.080 16 5083744 frameshift variant -/TG ins 1.3E-05; 8.5E-06 2.1E-05 2
rs151173406 1.000 0.080 16 5078842 missense variant C/T snv 8.0E-06 2.8E-05 2
rs398124401 0.695 0.480 4 55346393 stop gained G/A snv 1.2E-04 2.8E-05 25