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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCNN1B
(S82C)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
SCNN1B
Single nucleotide variant
(intron variant)
not provided
+4 more
GBenign
SCNN1B
Single nucleotide variant
(synonymous variant)
Bronchiectasis with or without elevated sweat chloride 1
+3 more
GConflicting classifications of pathogenicity
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