ClinVar Miner

List of variants in gene NNT reported as likely pathogenic for Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency

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: 3

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HGVS	dbSNP
NM_182977.3(NNT):c.1575dup (p.Pro526fs)
NM_182977.3(NNT):c.598G>A (p.Gly200Ser)	rs886039788
NM_182977.3(NNT):c.98dup (p.Leu33fs)	rs1579966821

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