Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs773658037
rs773658037
LDLR ; MIR6886
0.810 GeneticVariation BEFREE Our results suggest that sEH R287Q</span> may have a role in the elevation of blood LDL in FH. 29665449

2018
dbSNP: rs773658037
rs773658037
LDLR ; MIR6886
0.810 GeneticVariation UNIPROT Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. 27854360

2017
dbSNP: rs773658037
rs773658037
LDLR ; MIR6886
0.810 GeneticVariation UNIPROT ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. 25356965

2015
dbSNP: rs773658037
rs773658037
LDLR ; MIR6886
0.810 GeneticVariation UNIPROT Recommendations for the management of patients with familial hypercholesterolemia. 25404096

2015
dbSNP: rs773658037
rs773658037
LDLR ; MIR6886
0.810 GeneticVariation UNIPROT Management of familial hypercholesterolemia in children and adolescents. Position paper of the Polish Lipid Expert Forum. 24636176

2014
dbSNP: rs773658037
rs773658037
LDLR ; MIR6886
0.810 GeneticVariation UNIPROT Integrated guidance on the care of familial hypercholesterolaemia from the International FH Foundation. 24418289

2014
dbSNP: rs773658037
rs773658037
LDLR ; MIR6886
0.810 GeneticVariation UNIPROT Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society. 25053660

2014
dbSNP: rs773658037
rs773658037
LDLR ; MIR6886
0.810 GeneticVariation UNIPROT ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. 23788249

2013
dbSNP: rs773658037
rs773658037
LDLR ; MIR6886
0.810 GeneticVariation UNIPROT Management of familial heterozygous hypercholesterolemia: Position Paper of the Polish Lipid Expert Forum. 23725921

2013
dbSNP: rs773658037
rs773658037
LDLR ; MIR6886
0.810 GeneticVariation UNIPROT INTERIM guidelines for the diagnosis and management of familial hypercholesterolaemia. 22364837

2012
dbSNP: rs773658037
rs773658037
LDLR ; MIR6886
0.810 GeneticVariation UNIPROT Familial hypercholesterolemia: screening, diagnosis and management of pediatric and adult patients: clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia. 21600525

2011
dbSNP: rs773658037
rs773658037
LDLR ; MIR6886
0.810 GeneticVariation UNIPROT Guidelines for the diagnosis and management of heterozygous familial hypercholesterolemia. 15177124

2004
dbSNP: rs773658037
rs773658037
LDLR ; MIR6886
C 0.810 GeneticVariation CLINVAR