Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Identification of eight novel mutations in a collaborative analysis of a part of the second transmembrane domain of the CFTR gene. 7683628

1993
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Standards and guidelines for CFTR mutation testing. 12394352

2003
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Structures of a minimal human CFTR first nucleotide-binding domain as a monomer, head-to-tail homodimer, and pathogenic mutant. 20150177

2010
dbSNP: rs121908803
rs121908803
CFTR
T 0.820 GeneticVariation CLINVAR A protein sequence that can encode native structure by disfavoring alternate conformations. 11938353

2002
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Modulation of endocytic trafficking and apical stability of CFTR in primary human airway epithelial cultures. 20008117

2010
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Four adult patients with the missense mutation L206W and a mild cystic fibrosis phenotype. 8522333

1995
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Detection of novel and rare mutations in exon 4 of the cystic fibrosis gene by SSCP. 1284529

1992
dbSNP: rs121908803
rs121908803
CFTR
T 0.820 GeneticVariation CLINVAR These residues are conserved across species, and mutations of two (P99L and P205S) are associated with cystic fibrosis. 8663008

1996
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation BEFREE These residues are conserved across species, and mutations of two (P99L and P205S) are associated with cystic fibrosis. 8663008

1996
dbSNP: rs121908803
rs121908803
CFTR
T 0.820 GeneticVariation CLINVAR Dynamic association of proteasomal machinery with the centrosome. 10225950

1999
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT A specific cystic fibrosis mutation (T3381) associated with the phenotype of isolated hypotonic dehydration. 7543567

1995
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Cystic fibrosis pulmonary guidelines: chronic medications for maintenance of lung health. 17761616

2007
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Impact of the deltaF508 mutation in first nucleotide-binding domain of human cystic fibrosis transmembrane conductance regulator on domain folding and structure. 15528182

2005
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT A mutation in the cystic fibrosis transmembrane conductance regulator generates a novel internalization sequence and enhances endocytic rates. 12529365

2003
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Cystic Fibrosis Foundation evidence-based guidelines for management of infants with cystic fibrosis. 19914445

2009
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Cystic fibrosis pulmonary guidelines: pulmonary complications: hemoptysis and pneumothorax. 20675678

2010
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Mutation characterization of CFTR gene in 206 Northern Irish CF families: thirty mutations, including two novel, account for approximately 94% of CF chromosomes. 8956039

1996
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Good laboratory practices for biochemical genetic testing and newborn screening for inherited metabolic disorders. 22475884

2012
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Detection of three rare frameshift mutations in the cystic fibrosis gene in an African-American (CF444delA), an Italian (CF2522insC), and a Soviet (CF3821delT). 1710600

1991
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Novel missense mutation (G314R) in a cystic fibrosis patient with hepatic failure. 8829633

1996
dbSNP: rs121908803
rs121908803
CFTR
0.820 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: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Laboratory standards and guidelines for population-based cystic fibrosis carrier screening. 11280952

2001
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Abnormal regulatory interactions of I148T-CFTR and the epithelial Na+ channel in Xenopus oocytes. 16822950

2007
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Human Genetics Society of Australasia position statement: population-based carrier screening for cystic fibrosis. 25431289

2014
dbSNP: rs121908803
rs121908803
CFTR
0.820 GeneticVariation UNIPROT Guidelines on the early management of infants diagnosed with cystic fibrosis following newborn screening. 20605539

2010