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 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 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 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 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 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 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 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 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 CausalMutation disease CLINVAR Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction. 26036859 2016