RS121908767 CFTR
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What This Variant Does
"Known as 3199del6 or NM_000492.3:c.3067_3072delATAGTG, rs121908767 is considered a (rare) pathogenic...
Associated Conditions
Cystic fibrosis
Congenital bilateral aplasia of vas deferens from CFTR mutation
CFTR-related disorder
Bronchiectasis with or without elevated sweat chloride 1
Cystic fibrosis
Congenital bilateral aplasia of vas deferens from CFTR mutation
CFTR-related disorder
Bronchiectasis with or without elevated sweat chloride 1
Other Variants in CFTR