ClinVar Miner

List of variants in gene combination COMT, TXNRD2 reported as uncertain significance 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.2T>C (p.Met1Thr)	rs749057584	0.00016
NM_006440.5(TXNRD2):c.11T>C (p.Met4Thr)	rs1429174414

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