List of variants in gene combination CYP21A2, LOC106780800 reported as benign by Eurofins NTD LLC (GA)

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	gnomAD frequency
NM_000500.9(CYP21A2):c.188A>T (p.His63Leu)	rs9378252	0.00995
NM_000500.9(CYP21A2):c.1481G>A (p.Ser494Asn)	rs6473
NM_000500.9(CYP21A2):c.293-13C>A	rs6467

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