"Revvity Omics, Revvity"[submitter] AND "SCNN1B"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2435776	NM_000336.3(SCNN1B):c.1108G>A (p.Val370Ile)	SCNN1B (V370I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2689929	NM_000336.3(SCNN1B):c.1270+6C>T	SCNN1B	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 870735	NM_000336.3(SCNN1B):c.1542+1G>A	SCNN1B	Single nucleotide variant (splice donor variant)	not provided	GPathogenic/Likely pathogenic

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