Source: CURATED

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: rs199473684
rs199473684
0.925 0.160 X 101399747 3 prime UTR variant C/T snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs397515870
rs397515870
1.000 0.160 X 101400692 missense variant G/C;T snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs886039136
rs886039136
X 101403885 frameshift variant G/-;GG delins
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs267607004
rs267607004
0.925 0.040 10 110812304 missense variant G/A snv 1.4E-05
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs397516607
rs397516607
0.925 0.040 10 110821356 missense variant G/A snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1566147422
rs1566147422
12 110911146 frameshift variant AG/- del
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs751392310
rs751392310
12 110919103 inframe deletion CCT/- delins 7.0E-06
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs202024436
rs202024436
11 111908969 splice acceptor variant T/C snv 3.6E-05 2.1E-05
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs397516686
rs397516686
11 111911722 start lost C/T snv 6.7E-05 2.8E-05
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs786205436
rs786205436
0.882 0.080 11 112088972 missense variant A/G;T snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.710 1.000 1 2015 2015
dbSNP: rs111033559
rs111033559
0.925 0.040 6 118558946 missense variant C/T snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs397516784
rs397516784
0.925 0.080 6 118558957 inframe deletion AGA/- delins 1.4E-05
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 1.000 3 2006 2013
dbSNP: rs111033560
rs111033560
0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs730880492
rs730880492
1.000 0.160 X 120447993 frameshift variant -/TGTTG delins 5.5E-06; 5.5E-06
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1554398705
rs1554398705
7 128842906 frameshift variant -/C delins
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs778127887
rs778127887
3 14141613 stop gained C/T snv 1.6E-05 3.5E-05
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs267606976
rs267606976
1.000 0.080 7 151564203 missense variant A/G snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 1.000 2 2005 2014
dbSNP: rs121908987
rs121908987
0.742 0.200 7 151576412 missense variant C/A;G;T snv 4.0E-06
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs193922697
rs193922697
1.000 0.040 7 151576438 missense variant G/A;T snv 1.6E-05
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1057517686
rs1057517686
0.827 0.120 1 1529299 missense variant C/T snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 1.000 1 2016 2016
dbSNP: rs148515772
rs148515772
EMD
X 154380902 missense variant G/A snv 8.2E-05 8.5E-05
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1569552936
rs1569552936
TAZ
X 154420249 frameshift variant C/- delins
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1057518905
rs1057518905
1 155140104 missense variant A/T snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs56793579
rs56793579
0.851 0.240 1 156115102 missense variant C/G;T snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.710 1.000 3 2002 2010
dbSNP: rs267607571
rs267607571
0.882 0.160 1 156134458 missense variant G/A;T snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0