ClinVar Miner

List of variants in gene combination CYP11B1, LOC110673972 reported as likely benign for glucocorticoid-remediable aldosteronism

Included ClinVar conditions (2):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000497.4(CYP11B1):c.29G>A (p.Cys10Tyr)	rs6405	0.00049
NM_000497.4(CYP11B1):c.89G>A (p.Arg30Gln)	rs201103987	0.00014

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