Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs77932196
rs77932196
CFTR
0.840 GeneticVariation UNIPROT Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR. 25981758

2015
dbSNP: rs77932196
rs77932196
CFTR
0.840 GeneticVariation UNIPROT Human Genetics Society of Australasia position statement: population-based carrier screening for cystic fibrosis. 25431289

2014
dbSNP: rs77932196
rs77932196
CFTR
0.840 GeneticVariation UNIPROT Molecular testing for cystic fibrosis carrier status practice guidelines: recommendations of the National Society of Genetic Counselors. 24014130

2014
dbSNP: rs77932196
rs77932196
CFTR
A 0.840 CausalMutation CLINVAR Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene. 23974870

2013
dbSNP: rs77932196
rs77932196
CFTR
C 0.840 CausalMutation CLINVAR Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene. 23974870

2013
dbSNP: rs77932196
rs77932196
CFTR
0.840 GeneticVariation UNIPROT Good laboratory practices for biochemical genetic testing and newborn screening for inherited metabolic disorders. 22475884

2012
dbSNP: rs77932196
rs77932196
CFTR
0.840 GeneticVariation UNIPROT ACOG Committee Opinion No. 486: Update on carrier screening for cystic fibrosis. 21422883

2011
dbSNP: rs77932196
rs77932196
CFTR
C 0.840 CausalMutation CLINVAR Effects of gender and age at diagnosis on disease progression in long-term survivors of cystic fibrosis. 20448091

2010
dbSNP: rs77932196
rs77932196
CFTR
0.840 GeneticVariation UNIPROT Cystic fibrosis pulmonary guidelines: pulmonary complications: hemoptysis and pneumothorax. 20675678

2010
dbSNP: rs77932196
rs77932196
CFTR
0.840 GeneticVariation UNIPROT Guidelines on the early management of infants diagnosed with cystic fibrosis following newborn screening. 20605539

2010
dbSNP: rs77932196
rs77932196
CFTR
0.840 GeneticVariation UNIPROT Cystic Fibrosis Foundation evidence-based guidelines for management of infants with cystic fibrosis. 19914445

2009
dbSNP: rs77932196
rs77932196
CFTR
0.840 GeneticVariation UNIPROT ACOG Committee Opinion No. 442: Preconception and prenatal carrier screening for genetic diseases in individuals of Eastern European Jewish descent. 19888064

2009
dbSNP: rs77932196
rs77932196
CFTR
0.840 GeneticVariation UNIPROT Cystic Fibrosis Foundation practice guidelines for the management of infants with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome during the first two years of life and beyond. 19914443

2009
dbSNP: rs77932196
rs77932196
CFTR
C 0.840 CausalMutation CLINVAR Clinical practice and genetic counseling for cystic fibrosis and CFTR-related disorders. 19092437

2008
dbSNP: rs77932196
rs77932196
CFTR
C 0.840 CausalMutation CLINVAR Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice. 18456578

2008
dbSNP: rs77932196
rs77932196
CFTR
0.840 GeneticVariation UNIPROT Cystic fibrosis pulmonary guidelines: chronic medications for maintenance of lung health. 17761616

2007
dbSNP: rs77932196
rs77932196
CFTR
0.840 GeneticVariation UNIPROT Cystic fibrosis prenatal screening in genetic counseling practice: recommendations of the National Society of Genetic Counselors. 15789152

2005
dbSNP: rs77932196
rs77932196
CFTR
A 0.840 CausalMutation CLINVAR Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel. 15371902

2005
dbSNP: rs77932196
rs77932196
CFTR
C 0.840 CausalMutation CLINVAR Effect of genotype on phenotype and mortality in cystic fibrosis: a retrospective cohort study. 12767731

2003
dbSNP: rs77932196
rs77932196
CFTR
0.840 GeneticVariation UNIPROT Standards and guidelines for CFTR mutation testing. 12394352

2003
dbSNP: rs77932196
rs77932196
CFTR
0.840 GeneticVariation BEFREE This patient is also a compound heterozygote for the cystic fibrosis (CF) mutations, DeltaF508 and R347P. 12400067

2002
dbSNP: rs77932196
rs77932196
CFTR
C 0.840 CausalMutation CLINVAR Genotype and phenotype correlations in patients with cystic fibrosis and pancreatitis. 12454843

2002
dbSNP: rs77932196
rs77932196
CFTR
C 0.840 CausalMutation CLINVAR Laboratory standards and guidelines for population-based cystic fibrosis carrier screening. 11280952

2001
dbSNP: rs77932196
rs77932196
CFTR
0.840 GeneticVariation UNIPROT Laboratory standards and guidelines for population-based cystic fibrosis carrier screening. 11280952

2001
dbSNP: rs77932196
rs77932196
CFTR
C 0.840 CausalMutation CLINVAR High morbidity and mortality in cystic fibrosis patients compound heterozygous for 3905insT and deltaF508. 11491162

2001