Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909008
rs121909008
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.800 GeneticVariation UNIPROT A novel mutation in exon 12 (Y569C) of the CFTR gene identified in a patient of Croatian origin. 8723693

1996

dbSNP: rs121909008
rs121909008
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.800 GeneticVariation UNIPROT A specific cystic fibrosis mutation (T3381) associated with the phenotype of isolated hypotonic dehydration. 7543567

1995

dbSNP: rs121909008
rs121909008
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.800 GeneticVariation UNIPROT Four adult patients with the missense mutation L206W and a mild cystic fibrosis phenotype. 8522333

1995

dbSNP: rs121909008
rs121909008
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.800 GeneticVariation UNIPROT A novel cystic fibrosis mutation, Y109C, in the first transmembrane domain of CFTR. 7524909

1994

dbSNP: rs121909008
rs121909008
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.800 GeneticVariation UNIPROT Identification of three novel cystic fibrosis mutations in a sample of Italian cystic fibrosis patients. 8406518

1993

dbSNP: rs121909008
rs121909008
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.800 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: rs121909008
rs121909008
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.800 GeneticVariation UNIPROT Detection of novel and rare mutations in exon 4 of the cystic fibrosis gene by SSCP. 1284529

1992

dbSNP: rs121909008
rs121909008
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.800 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: rs121909008
rs121909008
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.800 GeneticVariation UNIPROT A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein. 1695717

1990