RS76713772 CFTR
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What This Variant Does
"rs76713772, also known as 1717-1G->
Associated Conditions
Cystic fibrosis
Congenital bilateral aplasia of vas deferens from CFTR mutation
CFTR-related disorder
Bronchiectasis with or without elevated sweat chloride 1
Hereditary pancreatitis
Cystic fibrosis
Congenital bilateral aplasia of vas deferens from CFTR mutation
CFTR-related disorder
Bronchiectasis with or without elevated sweat chloride 1
Hereditary pancreatitis
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Cerebrospinal fluid sTREM-2 levels | — | β: 10514.731 | 5E-6 | PubMed |
Other Variants in CFTR