Gene: MIR6886 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 CausalMutation disease CLINVAR Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction. 26036859 2016
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 CausalMutation disease CLINVAR RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease. 25525159 2015
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 CausalMutation disease CLINVAR Actionable exomic incidental findings in 6503 participants: challenges of variant classification. 25637381 2015
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 GeneticVariation disease CLINVAR Cardiovascular risk assessment of dyslipidemic children: analysis of biomarkers to identify monogenic dyslipidemia. 24627126 2014
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 CausalMutation disease CLINVAR Effects of intronic mutations in the LDLR gene on pre-mRNA splicing: Comparison of wet-lab and bioinformatics analyses. 19208450 2009
Entrez Id: 102465534
Gene Symbol: MIR6886
MIR6886 		0.100 GeneticVariation 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 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 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 Intronic mutations at splice junctions in the low-density lipoprotein receptor gene. 10441197 1999
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 Mutations in the low density lipoprotein receptor gene of familial hypercholesterolemic patients detected by denaturing gradient gel electrophoresis and direct sequencing. 7616128 1995