ClinVar Miner

List of variants reported as uncertain significance 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000336.3(SCNN1B):c.1760A>G (p.Asn587Ser)	rs769244277	0.00001
NM_000336.3(SCNN1B):c.1256A>T (p.Asp419Val)	rs1962882235
NM_001039.4(SCNN1G):c.637G>A (p.Asp213Asn)

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