ClinVar Miner

List of variants reported as likely pathogenic for adrenocortical insufficiency by Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_015665.6(AAAS):c.281del (p.Asn94fs)	rs2498627975
NM_015665.6(AAAS):c.771dup (p.Arg258fs)
NM_182977.3(NNT):c.2519_2522dup (p.Tyr841Ter)

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