List of variants in gene SCNN1G reported as likely benign for Liddle syndrome

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001039.4(SCNN1G):c.547G>A (p.Gly183Ser)	rs5736	0.01206
NM_001039.4(SCNN1G):c.435C>T (p.Ser145=)	rs62639702	0.00695
NM_001039.4(SCNN1G):c.589G>A (p.Glu197Lys)	rs5738	0.00548
NM_001039.4(SCNN1G):c.1570-9G>A	rs72647540	0.00354
NM_001039.4(SCNN1G):c.1589A>G (p.Asn530Ser)	rs148985177	0.00069
NM_001039.4(SCNN1G):c.699C>T (p.His233=)	rs192839222	0.00009
NM_001039.4(SCNN1G):c.1827G>C (p.Leu609Phe)	rs745715995	0.00008
NM_001039.4(SCNN1G):c.132C>T (p.Ile44=)	rs774767092	0.00005
NM_001039.4(SCNN1G):c.399G>A (p.Glu133=)	rs200985912	0.00004
NM_001039.4(SCNN1G):c.1455T>C (p.Thr485=)	rs1270059843	0.00001
NM_001039.4(SCNN1G):c.538C>T (p.Arg180Trp)	rs763601481	0.00001
NM_001039.4(SCNN1G):c.*597dup	rs566227302
NM_001039.4(SCNN1G):c.1078-17TGC[3]
NM_001039.4(SCNN1G):c.819G>C (p.Thr273=)	rs201341816

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