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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCNN1B
(S197T)
Single nucleotide variant
(missense variant)
Liddle syndrome 1
GLikely benign
SCNN1B
(G496V +1 more)
Single nucleotide variant
(missense variant)
Liddle syndrome 1
GUncertain significance