ClinVar Miner

List of variants reported as likely pathogenic for adrenocortical insufficiency by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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_000198.4(HSD3B2):c.1064G>A (p.Trp355Ter)	rs767128094	0.00001
NM_000102.4(CYP17A1):c.1435_1438dup (p.Pro480fs)	rs556794126

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