LDB3, LIM domain binding 3, 11155

N. diseases: 69; N. variants: 15
Disease: Cardiomyopathy, Familial Idiopathic ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3740346
rs3740346 		1.000 0.040 10 86692112 intron variant G/C snv 0.19 0.14
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		Cardiovascular Diseases 0.010 < 0.001 1 2020 2020
dbSNP: rs4468255
rs4468255 		1.000 0.040 10 86679248 intron variant G/A;C snv
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		Cardiovascular Diseases 0.010 1.000 1 2020 2020
dbSNP: rs56165849
rs56165849 		1.000 0.040 10 86681952 intron variant A/G snv 0.50
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		Cardiovascular Diseases 0.010 < 0.001 1 2020 2020