Gene: MIR6886 ×
Source: CLINVAR ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 GeneticVariation disease CLINVAR Mutations in the low density lipoprotein receptor gene of familial hypercholesterolemic patients detected by denaturing gradient gel electrophoresis and direct sequencing. 7616128 1995
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 CausalMutation disease CLINVAR Genetic variation at a splicing branch point in intron 9 of the low density lipoprotein (LDL)-receptor gene: a rare mutation that disrupts mRNA splicing in a patient with familial hypercholesterolaemia and a common polymorphism. 8872473 1996
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 GeneticVariation disease CLINVAR Mutational and genetic origin of LDL receptor gene mutations detected in both Belgian and Dutch familial hypercholesterolemics. 9254862 1997
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 CausalMutation disease CLINVAR Mutational and genetic origin of LDL receptor gene mutations detected in both Belgian and Dutch familial hypercholesterolemics. 9254862 1997
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 CausalMutation disease CLINVAR Mutant transcripts of the LDL receptor gene: mRNA structure and quantity. 10090473 1999
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 CausalMutation disease CLINVAR Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in The Netherlands. 10735632 2000
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 CausalMutation disease CLINVAR Molecular genetics of familial hypercholesterolemia in Spain: Ten novel LDLR mutations and population analysis. 11668640 2001
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 GeneticVariation disease CLINVAR Molecular genetics of familial hypercholesterolemia in Spain: Ten novel LDLR mutations and population analysis. 11668640 2001
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 GeneticVariation disease CLINVAR Intronic mutations outside of Alu-repeat-rich domains of the LDL receptor gene are a cause of familial hypercholesterolemia. 12436241 2002
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 GeneticVariation disease CLINVAR Comparison of SSCP and DHPLC for the detection of LDLR mutations in a New Zealand cohort. 11857755 2002
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 CausalMutation disease CLINVAR Comparison of SSCP and DHPLC for the detection of LDLR mutations in a New Zealand cohort. 11857755 2002
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 CausalMutation disease CLINVAR Molecular characterization of familial hypercholesterolemia in Spain: identification of 39 novel and 77 recurrent mutations in LDLR. 15241806 2004
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 GeneticVariation disease CLINVAR Application of molecular genetics for diagnosing familial hypercholesterolemia in Norway: results from a family-based screening program. 15199436 2004
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 CausalMutation disease CLINVAR Genetic diagnosis of familial hypercholesterolaemia: the importance of functional analysis of potential splice-site mutations. 19411563 2009
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 GeneticVariation disease CLINVAR Genetic diagnosis of familial hypercholesterolemia using a DNA-array based platform. 19318025 2009
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 CausalMutation disease CLINVAR Founder mutations in the Netherlands: geographical distribution of the most prevalent mutations in the low-density lipoprotein receptor and apolipoprotein B genes. 21475731 2011
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 CausalMutation disease CLINVAR Molecular basis of autosomal dominant hypercholesterolemia: assessment in a large cohort of hypercholesterolemic children. 21382890 2011
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 CausalMutation disease CLINVAR Cardiovascular risk in relation to functionality of sequence variants in the gene coding for the low-density lipoprotein receptor: a study among 29,365 individuals tested for 64 specific low-density lipoprotein-receptor sequence variants. 22390909 2012
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 GeneticVariation disease CLINVAR Whole-exome sequencing in an extended family with myocardial infarction unmasks familial hypercholesterolemia. 25154303 2014
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 CausalMutation disease CLINVAR Whole-exome sequencing in an extended family with myocardial infarction unmasks familial hypercholesterolemia. 25154303 2014
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 GeneticVariation disease CLINVAR Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction. 26036859 2016