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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CFTR
(E217G)
Single nucleotide variant
(missense variant)
CFTR-related disorder
+3 more
GConflicting classifications of pathogenicity
CFTR
(S912L)
Single nucleotide variant
(missense variant)
Cystic fibrosis
GUncertain significance
CFTR
(Q1352H)
Single nucleotide variant
(missense variant)
CFTR-related disorder
+3 more
GConflicting classifications of pathogenicity
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