Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852709
rs137852709
SCNN1B
0.800 GeneticVariation UNIPROT Genetic analysis of Rwandan patients with cystic fibrosis-like symptoms: identification of novel cystic fibrosis transmembrane conductance regulator and epithelial sodium channel gene variants. 19017867

2009
dbSNP: rs137852710
rs137852710
SCNN1B
0.800 GeneticVariation UNIPROT Genetic analysis of Rwandan patients with cystic fibrosis-like symptoms: identification of novel cystic fibrosis transmembrane conductance regulator and epithelial sodium channel gene variants. 19017867

2009
dbSNP: rs137852711
rs137852711
SCNN1B
0.800 GeneticVariation UNIPROT Genetic analysis of Rwandan patients with cystic fibrosis-like symptoms: identification of novel cystic fibrosis transmembrane conductance regulator and epithelial sodium channel gene variants. 19017867

2009
dbSNP: rs137852712
rs137852712
SCNN1B
0.800 GeneticVariation UNIPROT Genetic analysis of Rwandan patients with cystic fibrosis-like symptoms: identification of novel cystic fibrosis transmembrane conductance regulator and epithelial sodium channel gene variants. 19017867

2009
dbSNP: rs35731153
rs35731153
SCNN1B
0.800 GeneticVariation UNIPROT Genetic analysis of Rwandan patients with cystic fibrosis-like symptoms: identification of novel cystic fibrosis transmembrane conductance regulator and epithelial sodium channel gene variants. 19017867

2009
dbSNP: rs137852709
rs137852709
SCNN1B
0.800 GeneticVariation UNIPROT Could a defective epithelial sodium channel lead to bronchiectasis. 18507830

2008
dbSNP: rs137852710
rs137852710
SCNN1B
0.800 GeneticVariation UNIPROT Could a defective epithelial sodium channel lead to bronchiectasis. 18507830

2008
dbSNP: rs137852711
rs137852711
SCNN1B
0.800 GeneticVariation UNIPROT Could a defective epithelial sodium channel lead to bronchiectasis. 18507830

2008
dbSNP: rs137852712
rs137852712
SCNN1B
0.800 GeneticVariation UNIPROT Could a defective epithelial sodium channel lead to bronchiectasis. 18507830

2008
dbSNP: rs35731153
rs35731153
SCNN1B
0.800 GeneticVariation UNIPROT Could a defective epithelial sodium channel lead to bronchiectasis. 18507830

2008
dbSNP: rs137852709
rs137852709
SCNN1B
0.800 GeneticVariation UNIPROT Mutations in the beta-subunit of the epithelial Na+ channel in patients with a cystic fibrosis-like syndrome. 16207733

2005
dbSNP: rs137852710
rs137852710
SCNN1B
0.800 GeneticVariation UNIPROT Mutations in the beta-subunit of the epithelial Na+ channel in patients with a cystic fibrosis-like syndrome. 16207733

2005
dbSNP: rs137852711
rs137852711
SCNN1B
0.800 GeneticVariation UNIPROT Mutations in the beta-subunit of the epithelial Na+ channel in patients with a cystic fibrosis-like syndrome. 16207733

2005
dbSNP: rs137852712
rs137852712
SCNN1B
0.800 GeneticVariation UNIPROT Mutations in the beta-subunit of the epithelial Na+ channel in patients with a cystic fibrosis-like syndrome. 16207733

2005
dbSNP: rs35731153
rs35731153
SCNN1B
0.800 GeneticVariation UNIPROT Mutations in the beta-subunit of the epithelial Na+ channel in patients with a cystic fibrosis-like syndrome. 16207733

2005
dbSNP: rs137852709
rs137852709
SCNN1B
T 0.800 CausalMutation CLINVAR

dbSNP: rs137852710
rs137852710
SCNN1B
A 0.800 CausalMutation CLINVAR

dbSNP: rs137852711
rs137852711
SCNN1B
A 0.800 CausalMutation CLINVAR

dbSNP: rs137852712
rs137852712
SCNN1B
G 0.800 CausalMutation CLINVAR

dbSNP: rs35731153
rs35731153
SCNN1B
G 0.800 CausalMutation CLINVAR

dbSNP: rs113993959
rs113993959
CFTR
T 0.700 CausalMutation CLINVAR

dbSNP: rs121908752
rs121908752
CFTR
G 0.700 CausalMutation CLINVAR

dbSNP: rs121908753
rs121908753
CFTR
A 0.700 CausalMutation CLINVAR

dbSNP: rs121908759
rs121908759
CFTR
A 0.700 CausalMutation CLINVAR

dbSNP: rs121908761
rs121908761
CFTR
A 0.700 CausalMutation CLINVAR