Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs869312119
TTN ; TTN-AS1
1.000 0.040 2 178561756 stop gained G/A snv 2
rs869312118
TTN ; TTN-AS1
0.925 0.160 2 178562617 stop gained G/A snv 3
rs869312117
TTN-AS1 ; TTN
2 178568034 frameshift variant CTTT/- delins 1
rs869312116
TTN ; TTN-AS1
2 178571248 frameshift variant -/GTTT delins 4.0E-06 1
rs869312115
TTN-AS1 ; TTN
2 178573023 stop gained C/T snv 1
rs869312114
TTN ; TTN-AS1
2 178576255 stop gained C/A snv 1
rs869312113
TTN-AS1 ; TTN
2 178576752 frameshift variant AC/- delins 1
rs869312112
TTN ; TTN-AS1
0.925 0.160 2 178590230 stop gained G/A snv 3
rs869312111
TTN-AS1 ; TTN
2 178592653 frameshift variant A/- del 1
rs869312110
TTN-AS1 ; TTN
2 178598876 frameshift variant C/- delins 1
rs869312109
TTN-AS1 ; TTN
2 178599695 frameshift variant T/- del 1
rs869312108
TTN-AS1 ; TTN
2 178613825 stop gained C/T snv 1
rs869312107
TTN ; TTN-AS1
2 178618314 frameshift variant -/CA delins 1
rs869312106
TTN ; TTN-AS1
2 178633863 frameshift variant T/- delins 1
rs869312105
TTN ; TTN-AS1
2 178635489 stop gained A/C;G snv 1
rs869312104
TTN-AS1 ; TTN
2 178739177 frameshift variant T/- delins 1
rs869312103
TTN-AS1 ; TTN
2 178739333 stop gained C/A snv 1
rs869312102
TTN ; TTN-AS1
2 178741321 stop gained C/T snv 1
rs869312087
TTN ; TTN-AS1
2 178535593 frameshift variant CT/- delins 1
rs869312086
TTN-AS1 ; TTN
2 178536302 stop gained G/T snv 1
rs869312085
TTN ; TTN-AS1
2 178539559 stop gained G/A snv 8.0E-06 1
rs869312084
TTN-AS1 ; TTN
2 178543512 frameshift variant -/T delins 1
rs869312083
TTN-AS1 ; TTN
2 178546865 frameshift variant -/G delins 1
rs869312082
TTN-AS1 ; TTN
2 178552577 frameshift variant -/A ins 1
rs869312081
TTN-AS1 ; TTN
2 178552997 frameshift variant ATTA/- delins 8.1E-06 1