ClinVar Miner

List of variants in gene TXNRD2 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_006440.5(TXNRD2):c.375-19T>G	rs147120537	0.00527
NM_006440.5(TXNRD2):c.529-6C>T	rs116054286	0.00525

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