Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs386134243
LMNA
0.715 0.321 1 156135967 missense variant C/A,T snp 4.0E-06 14
rs574660186
TTN ; TTN-AS1
0.801 0.179 2 178579702 stop gained G/A snp 1.6E-05 3.2E-05 7
rs72646846
TTN-AS1 ; TTN
0.801 0.179 2 178589849 stop gained G/A snp 7.6E-05 3.2E-05 7
rs111033560
PLN ; CEP85L
0.784 0.071 6 118559037 stop gained T/G snp 1.6E-05 6
rs74315379
TNNT2
0.821 0.071 1 201364336 missense variant G/A,T snp 1.2E-04 6
rs137854607
SCN5A
0.801 0.107 3 38554309 missense variant C/G,T snp 5
rs137854618
SCN5A
0.734 0.107 3 38566426 missense variant C/A,T snp 8.0E-06 5
rs267607490
DES
0.878 0.143 2 219425734 missense variant C/T snp 4
rs397516089
MYH7
0.846 0.036 14 23429807 missense variant C/G,T snp 4
rs397516248
MYH7 ; MHRT
0.923 0.107 14 23415153 missense variant C/T snp 4
rs397516471
TNNT2
0.878 0.071 1 201363348 missense variant C/T snp 4
rs397517889
LMNA
0.878 0.143 1 156136093 missense variant C/T snp 4
rs45546039
SCN5A
0.769 0.107 3 38613781 missense variant C/A,T snp 4.1E-06 4
rs60682848
LMNA
0.846 0.143 1 156134838 stop gained C/T snp 4
rs104894655
TCAP
0.923 0.143 17 39665762 stop gained C/T snp 3
rs121908334
LDB3
0.923 0.107 10 86687218 missense variant C/T snp 4.0E-06 3
rs121912997
DSP
0.923 0.143 6 7579989 stop gained C/G,T snp 3
rs267607003
RBM20
0.923 0.036 10 110812310 missense variant C/A,G,T snp 3
rs267607004
RBM20
0.923 0.036 10 110812304 missense variant G/A snp 3
rs373040154
TTN-AS1 ; TTN
0.923 0.143 2 178617388 stop gained G/A,T snp 3.2E-05 3
rs387906875
BAG3
0.923 0.071 10 119670037 stop gained C/T snp 8.0E-06 3
rs397517689
TTN-AS1 ; TTN
0.923 0.036 2 178574530 stop gained G/A snp 4.0E-06 3
rs397517735
TTN-AS1 ; TTN
0.923 0.143 2 178559309 splice donor variant A/T snp 4.4E-06 3.2E-05 3
rs557312035
TTN-AS1 ; TTN
0.923 0.143 2 178564811 stop gained G/A,C,T snp 8.1E-06 3
rs56984562
LMNA
0.846 0.179 1 156137666 missense variant C/A,G,T snp 3