List of variants in gene combination CYP21A2, LOC106780800 reported as likely benign for Congenital adrenal hyperplasia

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000500.9(CYP21A2):c.342C>T (p.Ser114=)	rs193922546	0.00016
NM_000500.9(CYP21A2):c.327C>G (p.Ser109=)	rs193922545	0.00012
NM_000500.9(CYP21A2):c.1287C>T (p.Cys429=)	rs193922543

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