List of variants in gene SCNN1B reported as likely benign for bronchiectasis

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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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000336.3(SCNN1B):c.282C>T (p.Ala94=)	rs139950628	0.00551
NM_000336.3(SCNN1B):c.1731C>T (p.Thr577=)	rs61759923	0.00210
NM_000336.3(SCNN1B):c.1765G>A (p.Gly589Ser)	rs61759926	0.00180
NM_000336.3(SCNN1B):c.147A>G (p.Lys49=)	rs80027401	0.00141
NM_000336.3(SCNN1B):c.1152+10T>C	rs72654341	0.00108
NM_000336.3(SCNN1B):c.1190G>T (p.Arg397Leu)	rs61729789	0.00101
NM_000336.3(SCNN1B):c.1764T>C (p.Phe588=)	rs762486495	0.00024
NM_000336.2(SCNN1B):c.-150C>G	rs530631658	0.00022
NM_000336.3(SCNN1B):c.1299C>T (p.Ser433=)	rs149172890	0.00019
NM_000336.3(SCNN1B):c.1257C>T (p.Asp419=)	rs2303155	0.00016
NM_000336.3(SCNN1B):c.*20G>A	rs755277136	0.00010
NM_000336.3(SCNN1B):c.1789C>T (p.Arg597Cys)	rs373718332	0.00009
NM_000336.3(SCNN1B):c.1229G>A (p.Arg410His)	rs200966246	0.00007
NM_000336.3(SCNN1B):c.428C>T (p.Ser143Phe)	rs199810483	0.00006
NM_000336.3(SCNN1B):c.586-15T>C	rs371098444	0.00006
NM_000336.3(SCNN1B):c.177C>T (p.Phe59=)	rs778937866	0.00004
NM_000336.3(SCNN1B):c.246C>T (p.Ser82=)	rs757137077	0.00004
NM_000336.3(SCNN1B):c.617G>A (p.Arg206Gln)	rs201279350	0.00003
NM_000336.3(SCNN1B):c.1270+11G>T	rs369905217

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