Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs58978449
rs58978449
1 156134943 inframe deletion AAG/- delins
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 1.000 3 2000 2001
dbSNP: rs111569862
rs111569862
1 156137653 splice acceptor variant G/A;C snv
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 1.000 2 2008 2016
dbSNP: rs267607593
rs267607593
1 156134964 missense variant T/C snv
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 1.000 2 2003 2008
dbSNP: rs397517915
rs397517915
1 156135922 frameshift variant C/- del
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 1.000 2 2000 2012
dbSNP: rs58389804
rs58389804
1 156136049 frameshift variant T/- delins
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 1.000 2 2006 2011
dbSNP: rs397517904
rs397517904
1 156130774 splice donor variant G/A;C;T snv
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 1.000 1 2013 2013
dbSNP: rs397517909
rs397517909
1 156134949 stop gained G/T snv
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 1.000 1 2000 2000
dbSNP: rs59564495
rs59564495
1 156135231 frameshift variant G/- delins
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 1.000 1 2007 2007
dbSNP: rs794728593
rs794728593
1 156134933 synonymous variant G/A snv 7.0E-06
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 1.000 1 2017 2017
dbSNP: rs794728597
rs794728597
1 156130624 inframe deletion AAG/- delins
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 1.000 1 2012 2012
dbSNP: rs267607577
rs267607577
1 156136352 frameshift variant GCACGCAC/-;GCACGCACGCAC delins
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 0
dbSNP: rs397517886
rs397517886
1 156136070 missense variant T/C snv
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 0
dbSNP: rs397517887
rs397517887
1 156136074 inframe deletion ATGGAGATCCACGCC/- delins
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 0
dbSNP: rs397517895
rs397517895
1 156115072 missense variant C/G snv
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 0
dbSNP: rs397517908
rs397517908
1 156134927 frameshift variant C/- delins
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 0
dbSNP: rs397517911
rs397517911
1 156135239 missense variant C/G snv
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 0
dbSNP: rs730880132
rs730880132
1 156134875 missense variant T/C snv
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 0
dbSNP: rs753988867
rs753988867
1 156137180 missense variant C/T snv 2.1E-05 3.5E-05
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 0
dbSNP: rs876657650
rs876657650
1 156130736 frameshift variant A/- del
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 0
dbSNP: rs386134243
rs386134243
0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 1.000 11 2012 2017
dbSNP: rs60682848
rs60682848
0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.710 1.000 5 2001 2020
dbSNP: rs61195471
rs61195471
0.827 0.160 1 156134496 missense variant G/A snv
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 1.000 5 2001 2013
dbSNP: rs56984562
rs56984562
0.827 0.200 1 156137666 missense variant C/A;G;T snv
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 1.000 4 2003 2010
dbSNP: rs58596362
rs58596362
0.827 0.280 1 156138613 splice region variant C/A;T snv 8.1E-06
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 1.000 1 2003 2003
dbSNP: rs61444459
rs61444459
0.851 0.160 1 156137667 missense variant G/A;C snv
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 1.000 6 2003 2014