Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs868224085 1.000 0.040 2 221482474 missense variant G/A snv 1
rs267601191 1.000 0.040 7 100819817 missense variant G/A snv 1
rs1451501407 1.000 0.040 17 8006628 missense variant G/A snv 1
rs1238066548 1.000 0.040 19 38595699 missense variant G/A;T snv 1
rs267601046 1.000 0.040 6 43283303 missense variant C/T snv 1
rs745382803 1.000 0.040 3 69965076 missense variant C/A;G snv 4.0E-06; 4.0E-06 1
rs907102077 1.000 0.040 3 9760752 missense variant G/A snv 1
rs1484691555 1.000 0.040 20 9539512 missense variant C/T snv 4.0E-06 1
rs1277219458 1.000 0.040 2 241143002 missense variant C/T snv 1
rs779173667 1.000 0.040 4 54290418 missense variant G/A snv 8.0E-06 1.4E-05 1
rs267605306 1.000 0.040 19 14446504 missense variant C/G;T snv 1.6E-05 1
rs55735910 1.000 0.040 8 47881444 missense variant G/A snv 1.4E-05 1
rs267600891 1.000 0.040 6 166469882 missense variant C/T snv 1
rs755753950 1.000 0.040 22 40405688 missense variant G/A snv 4.4E-05 2.1E-05 1
rs564777385
TTN
1.000 0.040 2 178800635 missense variant C/G;T snv 3.6E-05 1
rs267599092 1.000 0.040 2 178779043 missense variant C/T snv 1
rs1204056923 1.000 0.040 2 178590160 missense variant C/T snv 1.4E-05 1
rs369098292 1.000 0.040 2 178572742 missense variant G/A snv 4.0E-06 1.4E-05 1
rs374713701 1.000 0.040 2 178593660 missense variant C/A;T snv 4.0E-06; 8.1E-06 1
rs1458591077 1.000 0.040 2 178630352 missense variant C/T snv 1
rs375422359 1.000 0.040 2 178563634 missense variant C/T snv 2.4E-05 3.5E-05 1
rs764005465 1.000 0.040 2 178572808 missense variant C/T snv 8.1E-06 1
rs121913368 0.925 0.040 7 140753345 missense variant AG/GA mnv 2
rs1024708183 0.925 0.040 19 7909761 missense variant A/G snv 4
rs750697353 0.882 0.080 3 12608919 missense variant C/T snv 1.2E-05 2.8E-05 4