ClinVar Miner

List of variants in gene combination AAAS, LOC130007973 reported as likely benign for adrenocortical insufficiency

Included ClinVar conditions (20):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_015665.6(AAAS):c.-70T>C	rs186975061

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