Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057516619 1.000 0.120 7 117536669 stop gained A/T snv 1
rs113857788 0.882 0.160 7 117664780 missense variant G/C;T snv 1.0E-03; 6.0E-05 3
rs113993958 0.882 0.200 7 117530953 missense variant G/A;C;T snv 2.0E-05; 4.0E-06 1
rs113993959 0.677 0.280 7 117587778 stop gained G/A;T snv 8.0E-06; 3.4E-04 8
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 3
rs121908751 0.925 0.160 7 117530899 stop gained G/A;T snv 4.0E-06 1
rs121908752 0.851 0.160 7 117535285 missense variant T/G snv 1.9E-04 1.3E-04 1
rs121908755 0.882 0.200 7 117587800 missense variant G/A;T snv 8.8E-05 2
rs121908757 0.925 0.160 7 117587799 missense variant A/C snv 4.0E-06 2
rs121908758 0.851 0.160 7 117590394 missense variant C/A snv 8.0E-06 7.0E-06 3
rs121908759 0.827 0.160 7 117592032 missense variant G/A snv 1.0E-04 3.8E-04 2
rs121908761 0.851 0.160 7 117611717 stop gained C/A;G snv 1.2E-05 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 2
rs121909010 1.000 0.120 7 117652915 stop gained G/A snv 1
rs121909011 0.807 0.160 7 117540230 missense variant C/T snv 5.6E-05 9.1E-05 3
rs121909019 0.925 0.160 7 117611638 missense variant G/A;T snv 3.2E-05 1
rs121909034 1.000 0.120 7 117603609 stop gained C/A;T snv 1.1E-03 1
rs121909044 0.925 0.200 7 117587812 missense variant G/A;C snv 4.0E-06 2
rs121909047 0.925 0.160 7 117590355 missense variant C/A snv 1.2E-05 2.1E-05 1
rs1396707015 1.000 0.120 7 117535273 stop gained G/A snv 1
rs139729994 0.925 0.120 7 117614713 missense variant G/A;T snv 4.0E-06; 1.3E-04 1
rs141033578 0.925 0.160 7 117606695 missense variant C/G;T snv 4.0E-06; 1.2E-05 1
rs142920240 0.851 0.240 7 117540273 missense variant T/A snv 1.4E-04 7.0E-05 5