List of variants in gene SCNN1A reported as likely benign for bronchiectasis with or without elevated sweat chloride 2

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_001038.6(SCNN1A):c.540G>T (p.Leu180=)	rs55859427	0.01886
NM_001038.6(SCNN1A):c.1477T>C (p.Trp493Arg)	rs5742912	0.01653
NM_001038.6(SCNN1A):c.684+9C>T	rs111317117	0.00378
NM_001038.6(SCNN1A):c.*4G>A	rs557017986	0.00014
NM_001038.6(SCNN1A):c.1074A>G (p.Glu358=)	rs149430403	0.00011
NM_001038.6(SCNN1A):c.1554A>G (p.Arg518=)	rs570566104	0.00010
NM_001038.6(SCNN1A):c.1394C>T (p.Ser465Phe)	rs369382063	0.00007
NM_001038.6(SCNN1A):c.1766G>A (p.Arg589Gln)	rs775290860	0.00004
NM_001038.6(SCNN1A):c.1805C>T (p.Ala602Val)	rs751903373	0.00004
NM_001038.6(SCNN1A):c.1801G>C (p.Gly601Arg)	rs755287192	0.00002
NM_001038.6(SCNN1A):c.540_541delinsTT (p.Arg181Trp)	rs876657425
NM_001038.6(SCNN1A):c.541C>T (p.Arg181Trp)	rs55797039

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