Gene: TAZ ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907218
rs387907218
TAZ
C 0.710 CausalMutation CLINVAR Infantile dilated X-linked cardiomyopathy, G4.5 mutations, altered lipids, and ultrastructural malformations of mitochondria in heart, liver, and skeletal muscle. 11896212

2002
dbSNP: rs387907218
rs387907218
TAZ
C 0.710 CausalMutation CLINVAR Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction. 12468278

2002
dbSNP: rs387907218
rs387907218
TAZ
C 0.710 CausalMutation CLINVAR The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies. 9382096

1997
dbSNP: rs387907218
rs387907218
TAZ
C 0.710 CausalMutation CLINVAR Two cases of endocardial fibroelastosis--possible x-linked determination. 4685904

1973
dbSNP: rs727504327
rs727504327
DNASE1L1 ; TAZ
A 0.700 GeneticVariation CLINVAR Barth syndrome mutations that cause tafazzin complex lability. 21300850

2011
dbSNP: rs727504327
rs727504327
DNASE1L1 ; TAZ
A 0.700 GeneticVariation CLINVAR Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome. 11238270

2001
dbSNP: rs1557194525
rs1557194525
TAZ
A 0.700 GeneticVariation CLINVAR

dbSNP: rs397515750
rs397515750
TAZ
T 0.700 GeneticVariation CLINVAR

dbSNP: rs727504394
rs727504394
TAZ
C 0.700 CausalMutation CLINVAR

dbSNP: rs727504431
rs727504431
TAZ
T 0.700 GeneticVariation CLINVAR