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: rs397516373
rs397516373
0.925 0.080 15 63059663 missense variant G/A snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 1.000 5 2016 2018
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: 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: 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: 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: rs769139957
rs769139957
15 84840691 frameshift variant C/-;CC delins
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 1.000 1 2017 2017
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: rs869125101
rs869125101
1.000 0.080 1 156134529 splice donor variant G/A;C snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 1.000 1 2013 2013
dbSNP: rs1057518905
rs1057518905
1 155140104 missense variant A/T snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1057519457
rs1057519457
19 35033599 missense variant A/T snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs111033559
rs111033559
0.925 0.040 6 118558946 missense variant C/T snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs121913628
rs121913628
0.763 0.160 14 23424059 missense variant C/G;T snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1242465339
rs1242465339
1.000 0.080 19 29207763 stop gained G/A;T snv 7.0E-06
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1425855043
rs1425855043
1.000 0.080 12 32878105 stop gained C/A snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1553644307
rs1553644307
0.925 0.160 2 178591418 stop gained T/A snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1553663867
rs1553663867
0.925 0.160 2 178598969 frameshift variant G/- del
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1553707780
rs1553707780
0.925 0.040 2 178616928 frameshift variant T/- del
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: rs1555122928
rs1555122928
1.000 0.080 11 47347434 frameshift variant C/- del
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1555142963
rs1555142963
12 32822477 frameshift variant TCCTGCTTCGACTGCCAAAACAT/- delins
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1555144459
rs1555144459
0.925 0.120 12 32841038 frameshift variant -/A delins
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1555661648
rs1555661648
0.882 0.240 18 26862297 missense variant C/G snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1559051231
rs1559051231
2 178535728 stop gained C/T snv
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1559192617
rs1559192617
2 178550977 frameshift variant CTTGTCATAAT/- delins
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0
dbSNP: rs1559262463
rs1559262463
2 178558000 frameshift variant A/- del
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 0