ClinVar Miner

List of variants reported as likely benign for Liddle syndrome by Johns Hopkins Genomics, Johns Hopkins University

Included ClinVar conditions (6):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000336.3(SCNN1B):c.466C>T (p.Arg156Trp)	rs139310448	0.00132
NM_000336.3(SCNN1B):c.1706C>T (p.Ala569Val)	rs140927806	0.00051

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