ClinVar Miner

List of variants in gene TXNRD2 reported as likely pathogenic for glucocorticoid deficiency 5

Included ClinVar conditions (1):

Glucocorticoid deficiency 5

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.1341T>G (p.Tyr447Ter)	rs202059967	0.00006
NM_006440.5(TXNRD2):c.1321C>T (p.Arg441Ter)	rs200162480	0.00002

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