ClinVar Miner

List of variants reported as uncertain significance for adrenocortical insufficiency by Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein

Included ClinVar conditions (20):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_000500.9(CYP21A2):c.104C>T (p.Pro35Leu)	rs200648381	0.00023
NM_000500.9(CYP21A2):c.37C>A (p.Leu13Met)	rs758864534

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