Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113993958 0.882 0.200 7 117530953 missense variant G/A;C;T snv 2.0E-05; 4.0E-06 2
rs115545701 0.925 0.160 7 117509089 missense variant C/T snv 1.5E-03 4.3E-03 2
rs11971167 0.882 0.160 7 117642528 missense variant G/A;T snv 1.3E-03 2
rs121908752 0.851 0.160 7 117535285 missense variant T/G snv 1.9E-04 1.3E-04 2
rs121909011 0.807 0.160 7 117540230 missense variant C/T snv 5.6E-05 9.1E-05 2
rs151048781 0.925 0.160 7 117603730 missense variant G/A;C snv 5.6E-05; 8.0E-05 2
rs1800097 0.925 0.160 7 117590357 missense variant G/A;C snv 1.4E-04; 4.8E-05 2
rs1800111 0.882 0.160 7 117610521 missense variant G/C snv 2.3E-03 2.1E-03 2
rs397508759 0.851 0.160 7 117534363 stop gained G/A;T snv 4.0E-06 2
rs75541969 0.827 0.200 7 117614699 missense variant G/C snv 4.0E-04 3.2E-04 2
rs78655421 0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 2
rs1177201180 1.000 0.120 7 117592160 missense variant A/T snv 1
rs121908750 1.000 0.120 7 117509140 missense variant G/A snv 4.0E-06 1
rs121908751 0.925 0.160 7 117530899 stop gained G/A;T snv 4.0E-06 1
rs121908753 0.851 0.160 7 117540285 missense variant G/A snv 2.4E-05 1
rs121908755 0.882 0.200 7 117587800 missense variant G/A;T snv 8.8E-05 1
rs121908758 0.851 0.160 7 117590394 missense variant C/A snv 8.0E-06 7.0E-06 1
rs121908759 0.827 0.160 7 117592032 missense variant G/A snv 1.0E-04 3.8E-04 1
rs121908802 0.851 0.160 7 117535263 missense variant C/T snv 7.0E-06 1
rs121908803 0.925 0.160 7 117535281 missense variant C/A;T snv 4.0E-06 7.0E-06 1
rs121909005 0.851 0.160 7 117587801 missense variant T/A;C;G snv 4.0E-06; 8.0E-06 1
rs121909006 0.925 0.160 7 117590360 missense variant T/A;C;G snv 8.0E-06 1
rs121909008 0.925 0.160 7 117603612 missense variant A/G snv 4.0E-06 7.0E-06 1
rs121909013 1.000 0.120 7 117587805 missense variant G/A snv 4.0E-06 1
rs121909015 1.000 0.120 7 117642593 missense variant G/C snv 8.0E-06 1