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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCNN1G
(E197Q)
Single nucleotide variant
(missense variant)
Liddle syndrome 2
+1 more
GUncertain significance
SCNN1G
(E197K)
Single nucleotide variant
(missense variant)
not provided
+4 more
GBenign/Likely benign