List of variants in gene KCNJ5 reported as benign for Familial hyperaldosteronism

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_000890.5(KCNJ5):c.*1338del	rs144472942	0.47522
NM_000890.5(KCNJ5):c.*1338C>A	rs6590358	0.27661
NM_000890.5(KCNJ5):c.*378dup	rs397799938
NM_000890.5(KCNJ5):c.*861GTTTT[7]	rs36205004

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