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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCNN1G
(P603R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SCNN1G
(R138*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
SCNN1G
(S467N)
Single nucleotide variant
(missense variant)
Bronchiectasis with or without elevated sweat chloride 3
GUncertain significance
SCNN1G
(R48fs)
Duplication
(frameshift variant)
Pseudohypoaldosteronism, type IB1, autosomal recessive
+2 more
GLikely pathogenic
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