ClinVar Miner

List of variants reported as pathogenic for adrenocortical insufficiency by Breakthrough Genomics, Breakthrough Genomics

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.293-13C>G	rs6467
NM_000529.2(MC2R):c.459dup (p.Ile154fs)	rs1555619430

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