List of variants in gene NR3C1 reported as benign for adrenogenital syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000176.3(NR3C1):c.*3298G>T	rs6191	0.48065
NM_000176.3(NR3C1):c.1469-16G>T	rs6188	0.29351
NM_000176.3(NR3C1):c.2298T>C (p.Asn766=)	rs6196	0.15759
NM_000176.3(NR3C1):c.*3833A>G	rs6198	0.11482
NM_000176.3(NR3C1):c.2034C>T (p.Asp678=)	rs258751	0.03733
NM_000176.3(NR3C1):c.66G>A (p.Glu22=)	rs6189	0.01685
NM_000176.3(NR3C1):c.*2188A>G	rs6193	0.01524
NM_000176.3(NR3C1):c.1764C>T (p.His588=)	rs6194	0.00372

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