List of variants in gene SCNN1B reported as uncertain significance for tracheal disorder

Minimum submission review status:		Collection method:
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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: 32

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HGVS	dbSNP	gnomAD frequency
NM_000336.3(SCNN1B):c.245C>G (p.Ser82Cys)	rs35731153	0.00463
NM_000336.3(SCNN1B):c.*241G>A	rs529644900	0.00040
NM_000336.3(SCNN1B):c.*278C>T	rs549628659	0.00038
NM_000336.3(SCNN1B):c.803A>G (p.His268Arg)	rs138004955	0.00029
NM_000336.3(SCNN1B):c.903A>G (p.Ile301Met)	rs149667567	0.00021
NM_000336.3(SCNN1B):c.*94G>A	rs72654359	0.00018
NM_000336.3(SCNN1B):c.467G>A (p.Arg156Gln)	rs765336896	0.00008
NM_000336.3(SCNN1B):c.1894G>A (p.Glu632Lys)	rs140609339	0.00007
NM_000336.3(SCNN1B):c.1322T>C (p.Ile441Thr)	rs770635298	0.00006
NM_000336.3(SCNN1B):c.1713C>T (p.Tyr571=)	rs758251652	0.00004
NM_000336.3(SCNN1B):c.1732G>A (p.Val578Met)	rs745885983	0.00004
NM_000336.3(SCNN1B):c.1900G>C (p.Asp634His)	rs776613953	0.00004
NM_000336.3(SCNN1B):c.1904G>A (p.Ser635Asn)	rs13306629	0.00004
NM_000336.3(SCNN1B):c.1404+7C>T	rs1485041245	0.00003
NM_000336.3(SCNN1B):c.*187G>A	rs886051816	0.00002
NM_000336.3(SCNN1B):c.1199A>G (p.Asn400Ser)	rs768729700	0.00001
NM_000336.3(SCNN1B):c.159C>T (p.Phe53=)	rs749106839	0.00001
NM_000336.3(SCNN1B):c.561C>T (p.His187=)	rs773448523	0.00001
NM_000336.3(SCNN1B):c.753C>T (p.Phe251=)	rs748167291	0.00001
NM_000336.3(SCNN1B):c.*446C>A	rs1452320359
NM_000336.3(SCNN1B):c.1069C>A (p.Pro357Thr)	rs932297365
NM_000336.3(SCNN1B):c.1228C>T (p.Arg410Cys)	rs200401219
NM_000336.3(SCNN1B):c.1271-10T>C	rs886051814
NM_000336.3(SCNN1B):c.1328T>C (p.Met443Thr)
NM_000336.3(SCNN1B):c.1329G>A (p.Met443Ile)
NM_000336.3(SCNN1B):c.1336G>A (p.Glu446Lys)	rs1962919047
NM_000336.3(SCNN1B):c.1404+15G>A	rs886051815
NM_000336.3(SCNN1B):c.1745T>A (p.Val582Glu)	rs1963026711
NM_000336.3(SCNN1B):c.372G>T (p.Glu124Asp)
NM_000336.3(SCNN1B):c.530G>A (p.Ser177Asn)	rs748962184
NM_000336.3(SCNN1B):c.748C>G (p.Leu250Val)	rs1962399992
NM_000336.3(SCNN1B):c.776+9C>A	rs1962401157

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