List of variants in gene SCNN1A reported as benign for Liddle syndrome 3

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001038.6(SCNN1A):c.1987A>G (p.Thr663Ala)	rs2228576	0.75229
NM_001038.6(SCNN1A):c.1553+32G>A	rs3764875	0.62475
NM_001038.6(SCNN1A):c.99C>T (p.Pro33=)	rs13306619	0.00986
NM_001038.6(SCNN1A):c.541C>T (p.Arg181Trp)	rs55797039

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