Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs57508089
LMNA
1.000 0.080 1 156136110 synonymous variant C/T snv 3
rs61195471
LMNA
0.827 0.160 1 156134496 missense variant G/A snv 3
rs727502886
ACTN2
0.925 0.040 1 236719007 missense variant G/A snv 3
rs727503565
TTN-AS1 ; TTN
0.925 0.160 2 178574498 frameshift variant T/- delins 3
rs727503586
TTN ; TTN-AS1
0.925 0.160 2 178589508 stop gained A/T snv 3
rs727504531
TTN-AS1 ; TTN
0.925 0.160 2 178573463 frameshift variant A/- del 3
rs727504550
TTN-AS1 ; TTN
0.925 0.160 2 178539537 stop gained C/T snv 3
rs727504801
SCN5A
0.925 0.080 3 38560397 frameshift variant G/- delins 3
rs775186117
TTN ; TTN-AS1
0.925 0.160 2 178617393 stop gained G/A snv 3
rs794728602
LMNA
1.000 0.040 1 156115168 missense variant G/A snv 3
rs794729265
TTN-AS1 ; TTN
0.925 0.160 2 178612355 stop gained G/A snv 7.0E-06 3
rs869025545
TTN-AS1 ; TTN
0.925 0.160 2 178566448 stop gained G/A snv 3
rs869312112
TTN ; TTN-AS1
0.925 0.160 2 178590230 stop gained G/A snv 3
rs869312118
TTN ; TTN-AS1
0.925 0.160 2 178562617 stop gained G/A snv 3
rs876657634
BAG3
0.925 0.080 10 119672477 stop gained C/T snv 3
rs876657666
TTN-AS1 ; TTN
0.925 0.160 2 178588815 frameshift variant -/G delins 3
rs886040968
SLC12A2
1.000 0.040 5 128178664 frameshift variant GTCTGGTGGCT/- delins 3
rs974671846
TTN ; TTN-AS1
0.925 0.160 2 178592211 stop gained C/T snv 7.0E-06 3
rs1553603152
TTN ; TTN-AS1
1.000 0.040 2 178570586 stop gained G/T snv 2
rs1553742630
TTN ; TTN-AS1
1.000 0.080 2 178633900 frameshift variant -/C ins 2
rs1553974835
HAND2-AS1 ; HAND2
1.000 0.040 4 173529091 stop gained C/A snv 2
rs1554105614
DSP
1.000 0.080 6 7555773 stop gained C/T snv 2
rs1564664312
RBM20
1.000 0.040 10 110821333 missense variant T/A snv 2
rs199473161
SCN5A
1.000 0.080 3 38586038 missense variant G/A;T snv 2
rs267607002
RBM20
1.000 0.040 10 110812303 missense variant C/A;T snv 2