ClinVar Miner

List of variants reported as likely pathogenic for adrenocortical insufficiency by Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City

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.850A>G (p.Met284Val)	rs770199817	0.00007
NM_182977.3(NNT):c.98dup (p.Leu33fs)	rs1579966821

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