Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909011
rs121909011
CFTR
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis 		T 0.850 CausalMutation CLINVAR Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene. 23974870

2013
dbSNP: rs121909011
rs121909011
CFTR
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis 		T 0.850 CausalMutation CLINVAR Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel. 15371902

2005